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Items: 1 to 100 of 643

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
RAD51DBreast-ovarian cancer, familial 4risk factor
(Aug 7, 2011)
no assertion criteria provided
2.
RAD51DBreast-ovarian cancer, familial 4risk factor
(Aug 7, 2011)
no assertion criteria provided
3.
RAD51DBreast-ovarian cancer, familial 4risk factor
(Aug 7, 2011)
no assertion criteria provided
4.
RAD51DBreast-ovarian cancer, familial 4risk factor
(Aug 7, 2011)
no assertion criteria provided
5.
GRCh37:
Chr17:17711738-217748468
AANAT, ACACA, ASIC2, ACLY, ACOX1, ACTG1, AP2B1, ALDH3A1, ALDH3A2, ALDOC, AOC2, BIRC5, APOH, ARL4D, ARHGDIA, ATP5MC1, ATP6V0A1, BLMH, BRCA1, FMNL1, CA4, CACNB1, CACNG1, CD7, CD79B, CDC6, CDC27, CDK3, CHAD, CLTC, CCR7, CNP, COL1A1, COX11, CPD, CRHR1, CRYBA1, CSF3, CSH1, CSH2, CSHL1, CSNK1D, SLC25A10, CYB561, ACE, DDX5, DHX8, DLX3, DLX4, DRG2, DUSP3, ERBB2, ERN1, ETV4, EVI2A, EVI2B, EVPL, EZH1, BPTF, FASN, FDXR, FOXJ1, FLII, FLOT2, GAST, FZD2, G6PC, GAA, GALK1, GCGR, KAT2A, GFAP, GH1, GH2, GIP, GNGT2, CCR10, UTS2R, GPS1, GRB2, GRB7, GRN, GRIN2C, H3F3B, HCRT, HLF, HOXB1, HOXB2, HOXB3, HOXB4, HOXB5, HOXB6, HOXB7, HOXB8, HOXB9, HSD17B1, ICAM2, MRPL58, IFI35, IGFBP4, FOXK2, ITGA2B, ITGA3, ITGB3, ITGB4, JUP, KCNJ2, KCNJ12, KCNJ16, KPNB1, KPNA2, KRT9, KRT10, KRT12, KRT13, KRT14, KRT15, KRT16, KRT17, KRT19, KRT31, KRT32, KRT33A, KRT33B, KRT34, KRT35, LASP1, LGALS3BP, LGALS9, LHX1, LIG3, LLGL2, LLGL1, LPO, NBR1, MAFG, MAPT, ADAM11, MAP3K3, MEOX1, MFAP4, MLLT6, MPO, MPP2, MPP3, TRIM37, MYL4, MYO1D, NAGLU, NEUROD2, NF1, NFE2L1, NGFR, NME1, NME2, NMT1, NOS2, NPTX1, NSF, OMG, P4HB, PDE6G, PDK2, PECAM1, PEX12, PHB, PNMT, SEPT4, MED1, PPY, PRKAR1A, PRKCA, MAPK7, MAP2K3, MAP2K6, PRPSAP1, PRPSAP2, PSMB3, PYY, PSMC5, PSMD3, PSMD11, PSMD12, PYCR1, PCYT2, RAB5C, RAC3, RAD51C, RAD51D, RARA, RFNG, RPL19, RPL23A, RPL27, RPL38, MRPL12, RPS6KB1, SCN4A, CCL1, CCL2, CCL3, CCL3L1, CCL4, CCL5, CCL7, CCL8, CCL11, CCL13, CCL14, CCL15, CCL16, CCL18, CCL23, SDF2, SEC14L1, SECTM1, SRSF1, SRSF2, SGCA, SGSH, SHMT1, SLC4A1, SLC6A4, SMARCD2, SMARCE1, SUMO2, SOX9, SP2, SREBF1, SRP68, SSTR2, STAT3, STAT5A, STAT5B, SUPT4H1, SUPT6H, TADA2A, TBCD, TBX2, HNF1B, MLX, THRA, TIMP2, TK1, TNFAIP1, TOP2A, TOP3A, TRQ-TTG1-1, DNAJC7, TUBG1, UBTF, VTN, WNT3, WNT9B, PCGF2, TRIM25, VEZF1, RNF112, ZNF207, TAF15, RND2, COIL, AKAP1, EPX, AXIN2, PIP4K2B, SPOP, FOXN1, PPM1D, CNTNAP1, DGKE, CBX4, TCAP, SKAP1, DNAH17, AOC3, BECN1, KRT38, KRT37, KRT36, ABCC3, RGS9, GALR2, TMEM11, KSR1, CDK5R1, SPHK1, CACNA1G, HAP1, MAP3K14, SOCS3, SPAG9, SLC13A2, UNC119, MTMR4, SLC16A6, SLC16A5, SLC16A3, SYNGR2, HGS, TIAF1, NOG, TSPOAP1, CYTH1, ZNHIT3, EFTUD2, RPL23, SLC9A3R1, COG1, RECQL5, PGS1, TBX4, NPEPPS, GOSR1, CCL4L2, GOSR2, NR1D1, TRAF4, AATK, KIAA0100, ULK2, TBKBP1, TMEM94, EIF4A3, PLEKHM1, MED24, LRRC37A, MRC2, HELZ, MED13, HDAC5, TOM1L1, GJC1, TOB1, ALYREF, PSME3, EIF1, NBR2, SLC35B1, DCAF7, CALCOCO2, RAMP2, ABCA10, ABCA9, ABCA8, BAIAP2, ATP5PD, HOXB13, VAT1, APPBP2, FBXW10, P3H4, ST6GALNAC2, HEXIM1, SPAG5, IGF2BP1, GNA13, CCT6B, RAI1, GRAP, SEPT9, CD300C, C1QL1, RUNDC3A, STARD3, CBX1, RAB40B, TLK2, DDX52, DUSP14, KAT7, AKAP10, POLG2, NXPH3, SNF8, SYNRG, CD300A, TMC6, DDX42, CASC3, IKZF3, ZNF652, PPM1E, ARSG, EPN2, CEP131, SARM1, GPATCH8, GGA3, JMJD6, EXOC7, USP22, KCNH4, ABCA6, ABCA5, KCTD2, SUZ12, MMD, WBP2, CDC42EP4, FSCN2, NOL11, DHRS7B, KRT23, TMEM98, POLDIP2, TBC1D29P, TANC2, WSB1, NAT9, PITPNC1, ERAL1, NARF, AATF, OR4D1, B9D1, CACNG5, CACNG4, TUBG2, TMEM97, NKIRAS2, COA3, GIT1, SAP30BP, PSMC3IP, SNX11, TBX21, NT5C, SOCS7, CDR2L, SOST, TVP23B, MRPS7, UTP18, RNFT1, JPT1, MYO15A, TUBD1, DCXR, RAPGEFL1, TACO1, ABI3, COPZ2, MRPL27, PIPOX, AMZ2, ARL17A, CRLF3, ANAPC11, SIRT7, SLC25A39, MRPS23, PTRH2, NLK, LUC7L3, HIGD1B, CDK12, KRT20, NLE1, SDK2, FNDC8, FAM20A, MBTD1, BCAS3, TMEM104, CWC25, ALKBH5, RNF43, MKS1, C17orf80, CCDC40, EPN3, WIPI1, SLFN12, PNPO, KLHL11, SMG8, SLC47A1, TMEM100, RHOT1, RSAD1, COPRS, LRRC59, NPLOC4, FAM222B, PRR11, ADAP2, ST6GALNAC1, UTP6, TEX2, GSDMB, GPRC5C, TEX14, WDR45B, CA10, ATXN7L3, CCDC47, PLXDC1, LYZL6, CBX8, MIF4GD, INTS2, CASKIN2, RPTOR, NUFIP2, TAOK1, BAHCC1, USP36, ARHGAP23, PHF12, RNF213, TNRC6C, PCTP, SCPEP1, SLC25A19, FKBP10, UBE2O, HEATR6, DUS1L, FN3K, XYLT2, C17orf75, DNAI2, SMURF2, ENGASE, SPATA20, MRPL38, UBE2Z, WNK4, C17orf53, GID4, ASPSCR1, TMUB2, CARD14, DHX58, MMP28, DHRS11, MFSD11, PRR15L, CYBC1, ARMC7, CHMP6, RHBDF2, DHX40, FN3KRP, OGFOD3, TEFM, ZNF750, ACBD4, DCAKD, GGNBP2, NUP85, ATAD5, MRM1, PLEKHH3, DBF4B, MYO19, ACSF2, FAAP100, CDK5RAP3, SP6, COASY, SRCIN1, AARSD1, LIMD2, KCNH6, FAM117A, VMP1, KRTAP1-3, KRTAP1-1, KRTAP9-9, KRTAP4-6, KRTAP2-1, DRC3, TTC25, KRTAP4-12, RAB34, TSPAN10, KRTAP1-5, KRTAP3-1, KRTAP3-2, KRTAP9-2, KRTAP9-3, KRTAP9-8, KRTAP17-1, BRIP1, MYCBPAP, QRICH2, NSRP1, PPP1R1B, TBC1D3F, RNF135, MIEN1, MRPL45, VPS25, TMEM101, PRAC1, RAB11FIP4, GHDC, KRTAP4-4, KIF2B, USP32, PPP1R9B, CBX2, FAM104A, CORO6, TNS4, FBXL20, KRTAP9-4, KRTAP4-1, KRTAP4-5, KRTAP4-3, KRTAP4-2, KRTAP3-3, KRTAP2-4, FBF1, UNK, SSH2, TP53I13, IFT20, LRRC46, SCRN2, CEP95, TRIM47, ANKRD40, ZNF830, SLFN11, RASL10B, ATPAF2, STRADA, PRR29, SPECC1, G6PC3, ASB16, OTOP2, PGAP3, PIGS, TTYH2, HSPB9, ORMDL3, PLCD3, SLC46A1, TMEM106A, LRRC37B, CYGB, RNF157, OSBPL7, C1QTNF1, NT5C3B, ABHD15, TLCD1, PPP1R27, FTSJ3, RFFL, METTL23, HSF5, OR4D2, MSI2, SLC38A10, CANT1, USH1G, CD300LB, KIF19, ZPBP2, C17orf64, SPATA32, HEXIM2, LSM12, CCDC43, CNTD1, TMEM132E, WFIKKN2, B4GALNT2, SPACA3, SEZ6, ANKRD13B, EFCAB13, MRPL10, TBC1D16, AFMID, GJD3, KRT222, KRT40, MIEF2, SLC5A10, DYNLL2, SMCR8, MGAT5B, TOM1L2, TEPSIN, B3GNTL1, RBFOX3, CD300LF, C17orf77, EFCAB3, SLC47A2, C17orf50, SLFN13, SLC35G3, UNC45B, CD300LG, KIF18B, RUNDC1, EME1, TMEM199, PROCA1, DHRS13, NOTUM, TMC8, TRIM16L, WIPF2, KRT25, TMEM99, ANKFN1, MARCH10, SLFN5, NAGS, RETREG3, TMEM92, PHOSPHO1, RHBDL3, SPPL2C, KRT28, KRT24, CEP112, ARHGAP27, ZNF385C, SAMD14, LYRM9, CENPX, LRRC45, SLC39A11, TRIM65, UNC13D, RDM1, GAS2L2, STH, STXBP4, TBC1D28, TAC4, MYADML2, CDRT15L2, NATD1, NPB, HEATR9, FADS6, HID1, TSEN54, UBALD2, TMEM235, CCDC57, HEXD, C17orf58, MILR1, KANSL1, CFAP97D1, FAM171A2, MEIOC, TTLL6, C17orf47, NEK8, PIGW, C17orf78, CISD3, GSDMA, CAVIN1, SLC26A11, ENDOV, GDPD1, NDUFAF8, TMEM105, LGALS9B, METRNL, KLHL10, RAB37, METTL2A, CCDC144NL, C17orf67, ENPP7, OXLD1, CCDC137, ARL16, C17orf51, MSL1, CD300E, NACA2, KRT27, SLFN14, STAC2, OTOP3, SKA2, MCRIP1, GPR142, ZACN, KRT26, PRAC2, EFCAB5, LRRC37A3, TMIGD1, CCL4L1, C17orf98, CCDC103, RPRML, YPEL2, C17orf82, BTBD17, ARL5C, KRT39, MYO18A, GRAPL, C17orf102, TEX19, CUEDC1, MIR10A, MIR144, MIR152, MIR193A, MIR196A1, MIR21, TBC1D3B, TBC1D3C, CCL3L3, MXRA7, GPR179, MIR338, LRRC37A2, FBXO47, MIR451A, CPSF4L, SMIM5, FAM83G, EVPLL, SEBOX, KRTAP4-11, LGALS9C, NME1-NME2, MIR33B, KRTAP4-8, KRTAP1-4, KRTAP2-2, KRTAP9-1, ZNF286B, TBC1D3, TBC1D3H, KRTAP2-3, PRCD, SNORD3A, SMIM6, CD300LD, KRTAP4-9, KRTAP4-7, TEN1, C17orf99, EPOP, MTRNR2L1, LRRC3C, KRTAP9-7, KRTAP16-1, HEXD-IT1, ARL17B, C17orf112, SLFN12L, KRTAP9-6, PTGES3L, PTGES3L-AARSD1, LOC101927666
Smith-Magenis syndromePathogenic
(Nov 12, 2015)
criteria provided, single submitter
6.
GRCh37:
Chr17:33426890
GRCh38:
Chr17:35099871
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
7.
GRCh37:
Chr17:33427094-33427097
GRCh38:
Chr17:35100075-35100078
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
8.
GRCh37:
Chr17:33427257
GRCh38:
Chr17:35100238
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityLikely benign
(Jun 14, 2016)
criteria provided, single submitter
9.
GRCh37:
Chr17:33427262
GRCh38:
Chr17:35100243
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityLikely benign
(Jun 14, 2016)
criteria provided, single submitter
10.
GRCh37:
Chr17:33427417
GRCh38:
Chr17:35100398
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityLikely benign
(Jun 14, 2016)
criteria provided, single submitter
11.
GRCh37:
Chr17:33427538-33427539
GRCh38:
Chr17:35100519-35100520
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
12.
GRCh37:
Chr17:33427599
GRCh38:
Chr17:35100580
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityLikely benign
(Jun 14, 2016)
criteria provided, single submitter
13.
GRCh37:
Chr17:33427605
GRCh38:
Chr17:35100586
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityLikely benign
(Jun 14, 2016)
criteria provided, single submitter
14.
GRCh37:
Chr17:33427606
GRCh38:
Chr17:35100587
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityLikely benign
(Jun 14, 2016)
criteria provided, single submitter
15.
GRCh37:
Chr17:33427718
GRCh38:
Chr17:35100699
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
16.
GRCh37:
Chr17:33427818
GRCh38:
Chr17:35100799
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
17.
GRCh37:
Chr17:33427842
GRCh38:
Chr17:35100823
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityLikely benign
(Jun 14, 2016)
criteria provided, single submitter
18.
GRCh37:
Chr17:33427866
GRCh38:
Chr17:35100847
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityLikely benign
(Jun 14, 2016)
criteria provided, single submitter
19.
GRCh37:
Chr17:33427958-33427960
GRCh38:
Chr17:35100939-35100941
RAD51D, RAD51L3-RFFLnot specifiedLikely benign
(Aug 2, 2016)
criteria provided, single submitter
20.
GRCh37:
Chr17:33427965
GRCh38:
Chr17:35100946
RAD51D, RAD51L3-RFFLnot specified, Hereditary cancer-predisposing syndromeBenign/Likely benign
(Nov 8, 2016)
criteria provided, multiple submitters, no conflicts
21.
GRCh37:
Chr17:33427968
GRCh38:
Chr17:35100949
RAD51D, RAD51L3-RFFLnot specified, Hereditary cancer-predisposing syndromeConflicting interpretations of pathogenicity
(May 15, 2017)
criteria provided, conflicting interpretations
22.
GRCh37:
Chr17:33427976
GRCh38:
Chr17:35100957
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary breast and ovarian cancer syndrome, not specified,
Hereditary cancer-predisposing syndrome, Breast and Ovarian Cancer Susceptibility
Conflicting interpretations of pathogenicity
(Jul 2, 2018)
criteria provided, conflicting interpretations
23.
GRCh37:
Chr17:33427980
GRCh38:
Chr17:35100961
RAD51D, RAD51L3-RFFLnot provided, Hereditary cancer-predisposing syndromeUncertain significance
(Dec 20, 2016)
criteria provided, multiple submitters, no conflicts
24.
GRCh37:
Chr17:33427982
GRCh38:
Chr17:35100963
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4Uncertain significance
(May 16, 2018)
criteria provided, single submitter
25.
GRCh37:
Chr17:33427986
GRCh38:
Chr17:35100967
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary breast and ovarian cancer syndrome, not specified,
not provided, Hereditary cancer-predisposing syndrome
Uncertain significance
(Jul 2, 2018)
criteria provided, multiple submitters, no conflicts
26.
GRCh37:
Chr17:33427987
GRCh38:
Chr17:35100968
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeUncertain significance
(Jan 5, 2018)
criteria provided, multiple submitters, no conflicts
27.
GRCh37:
Chr17:33427993
GRCh38:
Chr17:35100974
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, not provided,
Hereditary cancer-predisposing syndrome
Conflicting interpretations of pathogenicity
(Nov 28, 2017)
criteria provided, conflicting interpretations
28.
GRCh37:
Chr17:33427996
GRCh38:
Chr17:35100977
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Jul 1, 2016)
criteria provided, single submitter
29.
GRCh37:
Chr17:33428000
GRCh38:
Chr17:35100981
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Oct 5, 2016)
criteria provided, single submitter
30.
GRCh37:
Chr17:33428000-33428004
GRCh38:
Chr17:35100981-35100985
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not provided, Hereditary cancer-predisposing syndrome
Uncertain significance
(Mar 12, 2018)
criteria provided, multiple submitters, no conflicts
31.
GRCh37:
Chr17:33428002
GRCh38:
Chr17:35100983
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, Hereditary cancer-predisposing syndrome
Likely benign
(Dec 13, 2017)
criteria provided, multiple submitters, no conflicts
32.
GRCh37:
Chr17:33428004
GRCh38:
Chr17:35100985
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, Hereditary cancer-predisposing syndrome
Conflicting interpretations of pathogenicity
(Jul 5, 2017)
criteria provided, conflicting interpretations
33.
GRCh37:
Chr17:33428005
GRCh38:
Chr17:35100986
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeLikely benign
(Jan 16, 2014)
criteria provided, single submitter
34.
GRCh37:
Chr17:33428007
GRCh38:
Chr17:35100988
RAD51D, RAD51L3-RFFLnot specified, Hereditary cancer-predisposing syndromeUncertain significance
(Oct 9, 2017)
criteria provided, multiple submitters, no conflicts
35.
GRCh37:
Chr17:33428013
GRCh38:
Chr17:35100994
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Apr 25, 2017)
criteria provided, single submitter
36.
GRCh37:
Chr17:33428014
GRCh38:
Chr17:35100995
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeLikely benign
(Mar 23, 2015)
criteria provided, single submitter
37.
GRCh37:
Chr17:33428015
GRCh38:
Chr17:35100996
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeUncertain significance
(Sep 30, 2017)
criteria provided, multiple submitters, no conflicts
38.
GRCh37:
Chr17:33428015
GRCh38:
Chr17:35100996
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Oct 13, 2014)
criteria provided, single submitter
39.
GRCh37:
Chr17:33428016
GRCh38:
Chr17:35100997
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Jul 18, 2014)
criteria provided, single submitter
40.
GRCh37:
Chr17:33428019
GRCh38:
Chr17:35101000
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeUncertain significance
(May 11, 2018)
criteria provided, multiple submitters, no conflicts
41.
GRCh37:
Chr17:33428026
GRCh38:
Chr17:35101007
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndrome, Breast and Ovarian Cancer SusceptibilityUncertain significance
(Aug 1, 2018)
criteria provided, multiple submitters, no conflicts
42.
GRCh37:
Chr17:33428027-33428035
GRCh38:
Chr17:35101008-35101016
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4Uncertain significance
(Dec 14, 2017)
criteria provided, single submitter
43.
GRCh37:
Chr17:33428027
GRCh38:
Chr17:35101008
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not provided, Hereditary cancer-predisposing syndrome
Uncertain significance
(Dec 7, 2017)
criteria provided, multiple submitters, no conflicts
44.
GRCh37:
Chr17:33428027
GRCh38:
Chr17:35101008
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary breast and ovarian cancer syndrome, not specified,
not provided, Hereditary cancer-predisposing syndrome
Conflicting interpretations of pathogenicity
(Aug 1, 2018)
criteria provided, conflicting interpretations
45.
GRCh37:
Chr17:33428028
GRCh38:
Chr17:35101009
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Aug 1, 2018)
criteria provided, single submitter
46.
GRCh37:
Chr17:33428030
GRCh38:
Chr17:35101011
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Apr 6, 2016)
criteria provided, single submitter
47.
GRCh37:
Chr17:33428030
GRCh38:
Chr17:35101011
RAD51D, RAD51L3-RFFLBreast and Ovarian Cancer SusceptibilityUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
48.
GRCh37:
Chr17:33428034
GRCh38:
Chr17:35101015
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Jun 9, 2017)
criteria provided, single submitter
49.
GRCh37:
Chr17:33428035
GRCh38:
Chr17:35101016
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Jun 10, 2016)
criteria provided, single submitter
50.
GRCh37:
Chr17:33428037
GRCh38:
Chr17:35101018
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeConflicting interpretations of pathogenicity
(Apr 15, 2018)
criteria provided, conflicting interpretations
51.
GRCh37:
Chr17:33428038
GRCh38:
Chr17:35101019
RAD51D, RAD51L3-RFFLnot specifiedLikely benign
(Sep 8, 2016)
criteria provided, single submitter
52.
GRCh37:
Chr17:33428040
GRCh38:
Chr17:35101021
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary breast and ovarian cancer syndrome, not specified,
not provided, Hereditary cancer-predisposing syndrome
Conflicting interpretations of pathogenicity
(Jul 2, 2018)
criteria provided, conflicting interpretations
53.
GRCh37:
Chr17:33428041
GRCh38:
Chr17:35101022
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Mar 9, 2017)
criteria provided, single submitter
54.
GRCh37:
Chr17:33428044
GRCh38:
Chr17:35101025
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Apr 13, 2017)
criteria provided, single submitter
55.
GRCh37:
Chr17:33428048
GRCh38:
Chr17:35101029
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not provided, Hereditary cancer-predisposing syndrome
Uncertain significance
(Apr 20, 2018)
criteria provided, multiple submitters, no conflicts
56.
GRCh37:
Chr17:33428049
GRCh38:
Chr17:35101030
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeUncertain significance
(Nov 8, 2017)
criteria provided, multiple submitters, no conflicts
57.
GRCh37:
Chr17:33428052
GRCh38:
Chr17:35101033
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Oct 31, 2014)
criteria provided, single submitter
58.
GRCh37:
Chr17:33428054
GRCh38:
Chr17:35101035
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4Uncertain significance
(Aug 24, 2017)
criteria provided, single submitter
59.
GRCh37:
Chr17:33428057
GRCh38:
Chr17:35101038
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeConflicting interpretations of pathogenicity
(Sep 20, 2017)
criteria provided, conflicting interpretations
60.
GRCh37:
Chr17:33428058
GRCh38:
Chr17:35101039
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary breast and ovarian cancer syndrome, not specified,
not provided, Hereditary cancer-predisposing syndrome
Conflicting interpretations of pathogenicity
(Jul 2, 2018)
criteria provided, conflicting interpretations
61.
GRCh37:
Chr17:33428059-33428061
GRCh38:
Chr17:35101040-35101042
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, Hereditary cancer-predisposing syndrome
Benign/Likely benign
(Dec 8, 2017)
criteria provided, multiple submitters, no conflicts
62.
GRCh37:
Chr17:33428064
GRCh38:
Chr17:35101045
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeLikely benign
(Dec 5, 2016)
criteria provided, single submitter
63.
GRCh37:
Chr17:33428066
GRCh38:
Chr17:35101047
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, Hereditary cancer-predisposing syndrome
Likely benign
(Oct 6, 2017)
criteria provided, multiple submitters, no conflicts
64.
GRCh37:
Chr17:33428072
GRCh38:
Chr17:35101053
RAD51D, RAD51L3-RFFLnot specifiedLikely benign
(Jan 24, 2017)
criteria provided, single submitter
65.
GRCh37:
Chr17:33428222
GRCh38:
Chr17:35101203
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeConflicting interpretations of pathogenicity
(Jun 4, 2018)
criteria provided, conflicting interpretations
66.
GRCh37:
Chr17:33428223
GRCh38:
Chr17:35101204
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, Hereditary cancer-predisposing syndrome
Likely benign
(Jan 31, 2018)
criteria provided, multiple submitters, no conflicts
67.
GRCh37:
Chr17:33428224
GRCh38:
Chr17:35101205
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary breast and ovarian cancer syndrome, not provided,
Hereditary cancer-predisposing syndrome
Uncertain significance
(Jul 2, 2018)
criteria provided, multiple submitters, no conflicts
68.
GRCh37:
Chr17:33428225
GRCh38:
Chr17:35101206
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeLikely pathogenic
(Jan 20, 2017)
criteria provided, multiple submitters, no conflicts
69.
GRCh37:
Chr17:33428225
GRCh38:
Chr17:35101206
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary breast and ovarian cancer syndrome, not provided,
Hereditary cancer-predisposing syndrome
Likely pathogenic
(Jul 2, 2018)
criteria provided, multiple submitters, no conflicts
70.
GRCh37:
Chr17:33428234
GRCh38:
Chr17:35101215
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Mar 21, 2017)
criteria provided, single submitter
71.
GRCh37:
Chr17:33428235
GRCh38:
Chr17:35101216
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeLikely benign
(Aug 20, 2017)
criteria provided, multiple submitters, no conflicts
72.
GRCh37:
Chr17:33428237
GRCh38:
Chr17:35101218
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4Uncertain significance
(Jun 13, 2018)
criteria provided, single submitter
73.
GRCh37:
Chr17:33428238
GRCh38:
Chr17:35101219
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeConflicting interpretations of pathogenicity
(Mar 14, 2017)
criteria provided, conflicting interpretations
74.
GRCh37:
Chr17:33428240
GRCh38:
Chr17:35101221
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not provided, Hereditary cancer-predisposing syndrome
Uncertain significance
(Mar 6, 2018)
criteria provided, multiple submitters, no conflicts
75.
GRCh37:
Chr17:33428244
GRCh38:
Chr17:35101225
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeLikely benign
(May 9, 2017)
criteria provided, multiple submitters, no conflicts
76.
GRCh37:
Chr17:33428244
GRCh38:
Chr17:35101225
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeLikely benign
(Jul 31, 2017)
criteria provided, multiple submitters, no conflicts
77.
GRCh37:
Chr17:33428244
GRCh38:
Chr17:35101225
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, Hereditary cancer-predisposing syndrome
Likely benign
(Oct 26, 2017)
criteria provided, multiple submitters, no conflicts
78.
GRCh37:
Chr17:33428245
GRCh38:
Chr17:35101226
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4Uncertain significance
(Apr 25, 2018)
criteria provided, single submitter
79.
GRCh37:
Chr17:33428245
GRCh38:
Chr17:35101226
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, not provided,
Hereditary cancer-predisposing syndrome
Conflicting interpretations of pathogenicity
(Mar 11, 2018)
criteria provided, conflicting interpretations
80.
GRCh37:
Chr17:33428246
GRCh38:
Chr17:35101227
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Nov 9, 2016)
criteria provided, single submitter
81.
GRCh37:
Chr17:33428249
GRCh38:
Chr17:35101230
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4Uncertain significance
(Apr 19, 2017)
criteria provided, single submitter
82.
GRCh37:
Chr17:33428250
GRCh38:
Chr17:35101231
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, Hereditary cancer-predisposing syndrome,
Breast and Ovarian Cancer Susceptibility
Benign/Likely benign
(Jan 12, 2018)
criteria provided, multiple submitters, no conflicts
83.
GRCh37:
Chr17:33428251
GRCh38:
Chr17:35101232
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not provided, Hereditary cancer-predisposing syndrome
Uncertain significance
(Jun 19, 2018)
criteria provided, multiple submitters, no conflicts
84.
GRCh37:
Chr17:33428252
GRCh38:
Chr17:35101233
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Jun 30, 2017)
criteria provided, single submitter
85.
GRCh37:
Chr17:33428252
GRCh38:
Chr17:35101233
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeUncertain significance
(May 22, 2018)
criteria provided, multiple submitters, no conflicts
86.
GRCh37:
Chr17:33428254
GRCh38:
Chr17:35101235
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, Hereditary cancer-predisposing syndrome
Conflicting interpretations of pathogenicity
(May 13, 2018)
criteria provided, conflicting interpretations
87.
GRCh37:
Chr17:33428255
GRCh38:
Chr17:35101236
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, not provided,
Hereditary cancer-predisposing syndrome
Uncertain significance
(Jan 23, 2018)
criteria provided, multiple submitters, no conflicts
88.
GRCh37:
Chr17:33428258
GRCh38:
Chr17:35101239
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, Hereditary cancer-predisposing syndrome
Conflicting interpretations of pathogenicity
(Dec 19, 2017)
criteria provided, conflicting interpretations
89.
GRCh37:
Chr17:33428259
GRCh38:
Chr17:35101240
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, not provided,
Hereditary cancer-predisposing syndrome
Conflicting interpretations of pathogenicity
(Jan 3, 2018)
criteria provided, conflicting interpretations
90.
GRCh37:
Chr17:33428261
GRCh38:
Chr17:35101242
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary breast and ovarian cancer syndromeUncertain significance
(Jul 2, 2018)
criteria provided, multiple submitters, no conflicts
91.
GRCh37:
Chr17:33428269
GRCh38:
Chr17:35101250
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4Uncertain significance
(Dec 11, 2015)
criteria provided, single submitter
92.
GRCh37:
Chr17:33428273
GRCh38:
Chr17:35101254
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Oct 30, 2017)
criteria provided, single submitter
93.
GRCh37:
Chr17:33428274
GRCh38:
Chr17:35101255
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4Likely benign
(Dec 29, 2017)
criteria provided, single submitter
94.
GRCh37:
Chr17:33428279
GRCh38:
Chr17:35101260
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4Uncertain significance
(Jun 20, 2018)
criteria provided, single submitter
95.
GRCh37:
Chr17:33428280
GRCh38:
Chr17:35101261
RAD51D, RAD51L3-RFFLHereditary cancer-predisposing syndromeUncertain significance
(Jul 11, 2017)
criteria provided, single submitter
96.
GRCh37:
Chr17:33428280
GRCh38:
Chr17:35101261
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, Hereditary cancer-predisposing syndrome
Likely benign
(Sep 11, 2017)
criteria provided, multiple submitters, no conflicts
97.
GRCh37:
Chr17:33428281
GRCh38:
Chr17:35101262
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeUncertain significance
(Apr 26, 2018)
criteria provided, multiple submitters, no conflicts
98.
GRCh37:
Chr17:33428283
GRCh38:
Chr17:35101264
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary cancer-predisposing syndromeLikely benign
(Aug 31, 2016)
criteria provided, multiple submitters, no conflicts
99.
GRCh37:
Chr17:33428284
GRCh38:
Chr17:35101265
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, Hereditary breast and ovarian cancer syndrome, Hereditary cancer-predisposing syndrome
Uncertain significance
(Jul 2, 2018)
criteria provided, multiple submitters, no conflicts
100.
GRCh37:
Chr17:33428288
GRCh38:
Chr17:35101269
RAD51D, RAD51L3-RFFLBreast-ovarian cancer, familial 4, not specified, Hereditary cancer-predisposing syndrome
Uncertain significance
(May 3, 2018)
criteria provided, multiple submitters, no conflicts
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