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Items: 1 to 100 of 550

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review statusAccession
1.
GRCh37:
Chr3:10181832-10182443
GRCh38:
Chr3:10140148-10140759
VHLVon Hippel-Lindau syndromePathogenic
(Jun 1, 2020)
criteria provided, single submitterVCV000997768
2.
GRCh37:
Chr3:10183002
GRCh38:
Chr3:10141318
VHLnot providedBenign
(Jan 10, 2019)
criteria provided, single submitterVCV001178859
3.
GRCh37:
Chr3:10183241-10183242
GRCh38:
Chr3:10141557-10141558
VHLnot providedBenign
(Nov 19, 2019)
criteria provided, single submitterVCV001292417
4.
GRCh37:
Chr3:10183241-10183242
GRCh38:
Chr3:10141557-10141558
VHLnot providedBenign
(Nov 19, 2019)
criteria provided, single submitterVCV001267817
5.
GRCh37:
Chr3:10183274
GRCh38:
Chr3:10141590
VHLnot providedBenign
(Jan 10, 2019)
criteria provided, single submitterVCV001274684
6.
GRCh37:
Chr3:10183319-10183871
GRCh38:
Chr3:10141635-10142187
VHLErythrocytosis, familial, 2, Von Hippel-Lindau syndromePathogenic
(Oct 5, 2016)
criteria provided, single submitterVCV000417616
7.
GRCh37:
Chr3:10183325
GRCh38:
Chr3:10141641
VHLVon Hippel-Lindau syndromeUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000342396
8.
GRCh37:
Chr3:10183337
GRCh38:
Chr3:10141653
VHLnot provided, Von Hippel-Lindau syndrome, Erythrocytosis, familial, 2,
Von Hippel-Lindau syndrome
Benign
(Dec 2, 2020)
criteria provided, multiple submitters, no conflictsVCV000342397
9.
GRCh37:
Chr3:10183344
GRCh38:
Chr3:10141660
VHLVon Hippel-Lindau syndromeUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000900507
10.
GRCh37:
Chr3:10183353
GRCh38:
Chr3:10141669
VHLVon Hippel-Lindau syndromeUncertain significance
(Jan 17, 2018)
criteria provided, single submitterVCV000900508
11.
GRCh37:
Chr3:10183366
GRCh38:
Chr3:10141682
VHLVon Hippel-Lindau syndromeUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000342398
12.
GRCh37:
Chr3:10183407
GRCh38:
Chr3:10141723
VHLVon Hippel-Lindau syndromeUncertain significance
(Jun 14, 2016)
criteria provided, single submitterVCV000342399
13.
GRCh37:
Chr3:10183414
GRCh38:
Chr3:10141730
VHLVon Hippel-Lindau syndromeUncertain significance
(Feb 2, 2018)
criteria provided, single submitterVCV000902166
14.
GRCh37:
Chr3:10183435
GRCh38:
Chr3:10141751
VHLnot providedLikely benign
(May 31, 2019)
criteria provided, multiple submitters, no conflictsVCV000560737
15.
GRCh37:
Chr3:10183454-10183499
GRCh38:
Chr3:10141770-10141815
VHLnot provided, Von Hippel-Lindau syndromeUncertain significance
(Aug 23, 2016)
criteria provided, single submitterVCV000433541
16.
GRCh37:
Chr3:10183457-10183477
GRCh38:
Chr3:10141770-10141790
VHLVon Hippel-Lindau syndromeLikely pathogenic
(Dec 9, 2014)
criteria provided, single submitterVCV000166561
17.
GRCh37:
Chr3:10183455
GRCh38:
Chr3:10141771
VHLnot provided, not specified, Von Hippel-Lindau syndrome
Benign/Likely benign
(Mar 23, 2018)
criteria provided, multiple submitters, no conflictsVCV000256649
18.
GRCh37:
Chr3:10183459
GRCh38:
Chr3:10141775
VHLnot provided, Von Hippel-Lindau syndrome, Erythrocytosis, familial, 2,
Von Hippel-Lindau syndrome, Pheochromocytoma, Renal cell carcinoma, nonpapillary
Uncertain significance
(Oct 31, 2018)
criteria provided, multiple submitters, no conflictsVCV000560736
19.
GRCh37:
Chr3:10183466-10183467
GRCh38:
Chr3:10141782-10141783
VHLVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2, not specified,
not provided
Conflicting interpretations of pathogenicity
(Nov 21, 2020)
criteria provided, conflicting interpretationsVCV000517152
20.
GRCh37:
Chr3:10183468
GRCh38:
Chr3:10141784
VHLVon Hippel-Lindau syndrome, not providedConflicting interpretations of pathogenicity
(Aug 8, 2019)
criteria provided, conflicting interpretationsVCV000342400
21.
GRCh37:
Chr3:10183471-10183472
GRCh38:
Chr3:10141787-10141788
VHLHereditary cancer-predisposing syndromeUncertain significance
(Sep 16, 2014)
criteria provided, single submitterVCV000182985
22.
GRCh37:
Chr3:10183477
GRCh38:
Chr3:10141793
VHLnot providedUncertain significance
(Nov 28, 2017)
criteria provided, single submitterVCV000560735
23.
GRCh37:
Chr3:10183484
GRCh38:
Chr3:10141800
VHLnot specifiedLikely benign
(Jul 28, 2017)
criteria provided, single submitterVCV000511068
24.
GRCh37:
Chr3:10183485
GRCh38:
Chr3:10141801
VHLnot specifiedLikely benign
(Jul 27, 2017)
criteria provided, single submitterVCV000511159
25.
GRCh37:
Chr3:10183485
GRCh38:
Chr3:10141801
VHLnot specifiedLikely benign
(Jan 7, 2016)
criteria provided, single submitterVCV000382948
26.
GRCh37:
Chr3:10183487
GRCh38:
Chr3:10141803
VHLnot providedBenign
(Jul 13, 2015)
criteria provided, single submitterVCV001290627
27.
GRCh37:
Chr3:10183488
GRCh38:
Chr3:10141804
VHLnot specifiedLikely benign
(Feb 14, 2017)
criteria provided, single submitterVCV000507432
28.
GRCh37:
Chr3:10183492
GRCh38:
Chr3:10141808
VHLnot specifiedLikely benign
(Mar 15, 2016)
criteria provided, single submitterVCV000384826
29.
GRCh37:
Chr3:10183494
GRCh38:
Chr3:10141810
VHLnot specifiedLikely benign
(Jun 16, 2016)
criteria provided, single submitterVCV000380659
30.
GRCh37:
Chr3:10183496
GRCh38:
Chr3:10141812
VHLnot specifiedLikely benign
(Nov 3, 2017)
criteria provided, single submitterVCV000513189
31.
GRCh37:
Chr3:10183496
GRCh38:
Chr3:10141812
VHLnot specifiedLikely benign
(Aug 30, 2017)
criteria provided, single submitterVCV000511831
32.
GRCh37:
Chr3:10183497
GRCh38:
Chr3:10141813
VHLnot provided, Von Hippel-Lindau syndrome, not specified
Conflicting interpretations of pathogenicity
(Jan 12, 2018)
criteria provided, conflicting interpretationsVCV000137904
33.
GRCh37:
Chr3:10183502
GRCh38:
Chr3:10141818
VHLVon Hippel-Lindau syndromeUncertain significance
(Jun 14, 2016)
criteria provided, single submitterVCV000342401
34.
GRCh37:
Chr3:10183503
GRCh38:
Chr3:10141819
VHLnot specifiedLikely benign
(Jun 12, 2017)
criteria provided, single submitterVCV000389597
35.
GRCh37:
Chr3:10183506
GRCh38:
Chr3:10141822
VHLVon Hippel-Lindau syndromeUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000902167
36.
GRCh37:
Chr3:10183506
GRCh38:
Chr3:10141822
VHLnot specifiedBenign
(Mar 13, 2015)
criteria provided, single submitterVCV000378851
37.
GRCh37:
Chr3:10183507
GRCh38:
Chr3:10141823
VHLnot specifiedLikely benign
(Apr 3, 2017)
criteria provided, single submitterVCV000508543
38.
GRCh37:
Chr3:10183509
GRCh38:
Chr3:10141825
VHLnot providedLikely benign
(May 15, 2017)
criteria provided, single submitterVCV000560734
39.
GRCh37:
Chr3:10183516
GRCh38:
Chr3:10141832
VHLnot specifiedLikely benign
(Oct 27, 2016)
criteria provided, single submitterVCV000378852
40.
GRCh37:
Chr3:10183517-10183535
GRCh38:
Chr3:10141833-10141851
VHLM1fsnot providedUncertain significance
(Dec 19, 2019)
criteria provided, single submitterVCV001311090
41.
GRCh37:
Chr3:10183517
GRCh38:
Chr3:10141833
VHLnot specifiedLikely benign
(Nov 21, 2017)
criteria provided, single submitterVCV000381125
42.
GRCh37:
Chr3:10183519
GRCh38:
Chr3:10141835
VHLnot specifiedLikely benign
(May 16, 2016)
criteria provided, single submitterVCV000386209
43.
GRCh37:
Chr3:10183519-10183520
GRCh38:
Chr3:10141835-10141836
VHLM1fsnot providedLikely benign
(May 10, 2019)
criteria provided, single submitterVCV000279916
44.
GRCh37:
Chr3:10183521-10183522
GRCh38:
Chr3:10141837-10141838
VHLA5fsHereditary cancer-predisposing syndromeUncertain significance
(May 13, 2014)
criteria provided, single submitterVCV000182987
45.
GRCh37:
Chr3:10183522-10183881
GRCh38:
Chr3:10141838-10142197
VHLErythrocytosis, familial, 2, Von Hippel-Lindau syndromePathogenic
(Jun 24, 2019)
criteria provided, single submitterVCV000656836
46.
GRCh37:
Chr3:10183522
GRCh38:
Chr3:10141838
VHLnot specifiedLikely benign
(Jun 26, 2017)
criteria provided, single submitterVCV000510481
47.
GRCh37:
Chr3:10183527
GRCh38:
Chr3:10141843
VHLHereditary cancer-predisposing syndrome, not providedLikely benign
(Nov 26, 2020)
criteria provided, multiple submitters, no conflictsVCV000182989
48.
GRCh37:
Chr3:10183529
GRCh38:
Chr3:10141845
VHLHereditary cancer-predisposing syndromeUncertain significance
(May 10, 2018)
criteria provided, single submitterVCV000824483
49.
GRCh37:
Chr3:10183530
GRCh38:
Chr3:10141846
VHLHereditary cancer-predisposing syndromeUncertain significance
(May 3, 2018)
criteria provided, single submitterVCV000822530
50.
GRCh37:
Chr3:10183532
GRCh38:
Chr3:10141848
VHLM1VVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2, Von Hippel-Lindau syndrome
Uncertain significance
(Oct 22, 2019)
criteria provided, multiple submitters, no conflictsVCV000548790
51.
GRCh37:
Chr3:10183532
GRCh38:
Chr3:10141848
VHLM1Lnot provided, Von Hippel-Lindau syndrome, Erythrocytosis, familial, 2,
Von Hippel-Lindau syndrome
Uncertain significance
(Mar 30, 2021)
criteria provided, multiple submitters, no conflictsVCV000411967
52.
GRCh37:
Chr3:10183534
GRCh38:
Chr3:10141850
VHLM1IVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(May 9, 2018)
criteria provided, single submitterVCV000582995
53.
GRCh37:
Chr3:10183534
GRCh38:
Chr3:10141850
VHLM1IHereditary cancer-predisposing syndrome, Von Hippel-Lindau syndrome, Erythrocytosis, familial, 2,
not provided, Von Hippel-Lindau syndrome
Uncertain significance
(Sep 10, 2020)
criteria provided, multiple submitters, no conflictsVCV000238106
54.
GRCh37:
Chr3:10183534
GRCh38:
Chr3:10141850
VHLM1IErythrocytosis, familial, 2, Von Hippel-Lindau syndrome, Hereditary cancer-predisposing syndrome,
Von Hippel-Lindau syndrome, not specified, not provided
Uncertain significance
(Aug 28, 2020)
criteria provided, multiple submitters, no conflictsVCV000135406
55.
GRCh37:
Chr3:10183535
GRCh38:
Chr3:10141851
VHLR3fsHereditary cancer-predisposing syndromeUncertain significance
(Aug 22, 2018)
criteria provided, single submitterVCV000827380
56.
GRCh37:
Chr3:10183535
GRCh38:
Chr3:10141851
VHLP2AHereditary cancer-predisposing syndromeUncertain significance
(Jun 14, 2019)
criteria provided, single submitterVCV000825356
57.
GRCh37:
Chr3:10183535
GRCh38:
Chr3:10141851
VHLP2Snot provided, Von Hippel-Lindau syndrome, Erythrocytosis, familial, 2
Uncertain significance
(Oct 29, 2020)
criteria provided, multiple submitters, no conflictsVCV000574321
58.
GRCh37:
Chr3:10183536
GRCh38:
Chr3:10141852
VHLP2RVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(Aug 18, 2020)
criteria provided, single submitterVCV000411980
59.
GRCh37:
Chr3:10183536
GRCh38:
Chr3:10141852
VHLP2LErythrocytosis, familial, 2, Von Hippel-Lindau syndrome, not provided,
Hereditary cancer-predisposing syndrome, not specified, Von Hippel-Lindau syndrome
Conflicting interpretations of pathogenicity
(Oct 26, 2020)
criteria provided, conflicting interpretationsVCV000182981
60.
GRCh37:
Chr3:10183537-10183538
GRCh38:
Chr3:10141853-10141854
VHLR4fsHereditary cancer-predisposing syndromeUncertain significance
(Nov 12, 2018)
criteria provided, single submitterVCV000822886
61.
GRCh37:
Chr3:10183537
GRCh38:
Chr3:10141853
VHLVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2, not provided
Likely benign
(Dec 7, 2018)
criteria provided, single submitterVCV000759757
62.
GRCh37:
Chr3:10183537
GRCh38:
Chr3:10141853
VHLVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Likely benign
(Jan 13, 2017)
criteria provided, single submitterVCV000456593
63.
GRCh37:
Chr3:10183538
GRCh38:
Chr3:10141854
VHLR3GErythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Jun 10, 2020)
criteria provided, single submitterVCV001035825
64.
GRCh37:
Chr3:10183538
GRCh38:
Chr3:10141854
VHLR3WVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(Oct 21, 2020)
criteria provided, single submitterVCV000238114
65.
GRCh37:
Chr3:10183539-10183540
GRCh38:
Chr3:10141855-10141856
VHLA11fsnot providedUncertain significance
(Nov 12, 2020)
criteria provided, single submitterVCV001313664
66.
GRCh37:
Chr3:10183539
GRCh38:
Chr3:10141855
VHLR3PErythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Mar 25, 2018)
criteria provided, single submitterVCV000575760
67.
GRCh37:
Chr3:10183540
GRCh38:
Chr3:10141856
VHLVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Likely benign
(Jan 6, 2020)
criteria provided, single submitterVCV001103811
68.
GRCh37:
Chr3:10183541-10183542
GRCh38:
Chr3:10141857-10141858
VHLR4LHereditary cancer-predisposing syndromeUncertain significance
(Nov 28, 2018)
criteria provided, single submitterVCV000818240
69.
GRCh37:
Chr3:10183541
GRCh38:
Chr3:10141857
VHLR4WVon Hippel-Lindau syndromeUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000342402
70.
GRCh37:
Chr3:10183542
GRCh38:
Chr3:10141858
VHLR4MErythrocytosis, familial, 2, Von Hippel-Lindau syndrome, Von Hippel-Lindau syndrome
Uncertain significance
(May 25, 2020)
criteria provided, multiple submitters, no conflictsVCV000342403
71.
GRCh37:
Chr3:10183543
GRCh38:
Chr3:10141859
VHLErythrocytosis, familial, 2, Von Hippel-Lindau syndromeLikely benign
(Aug 25, 2020)
criteria provided, single submitterVCV000456572
72.
GRCh37:
Chr3:10183544
GRCh38:
Chr3:10141860
VHLA5PErythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Feb 19, 2018)
criteria provided, single submitterVCV000565618
73.
GRCh37:
Chr3:10183544-10183545
GRCh38:
Chr3:10141860-10141861
VHLE12fsnot providedUncertain significance
(Jan 18, 2017)
criteria provided, single submitterVCV000423088
74.
GRCh37:
Chr3:10183545
GRCh38:
Chr3:10141861
VHLA5VVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2, Von Hippel-Lindau syndrome,
Hereditary cancer-predisposing syndrome, not provided
Uncertain significance
(Jul 8, 2021)
criteria provided, multiple submitters, no conflictsVCV000216476
75.
GRCh37:
Chr3:10183546
GRCh38:
Chr3:10141862
VHLErythrocytosis, familial, 2, Von Hippel-Lindau syndromeLikely benign
(Oct 2, 2019)
criteria provided, single submitterVCV001138466
76.
GRCh37:
Chr3:10183547
GRCh38:
Chr3:10141863
VHLE6*Erythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Mar 9, 2020)
criteria provided, single submitterVCV001059764
77.
GRCh37:
Chr3:10183548
GRCh38:
Chr3:10141864
VHLE6AErythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Feb 12, 2019)
criteria provided, single submitterVCV000864304
78.
GRCh37:
Chr3:10183549
GRCh38:
Chr3:10141865
VHLVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Likely benign
(Apr 27, 2020)
criteria provided, single submitterVCV001157043
79.
GRCh37:
Chr3:10183549
GRCh38:
Chr3:10141865
VHLE6DVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(Nov 21, 2016)
criteria provided, single submitterVCV000411986
80.
GRCh37:
Chr3:10183550-10183551
GRCh38:
Chr3:10141866-10141867
VHLErythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Aug 17, 2020)
criteria provided, single submitterVCV001035305
81.
GRCh37:
Chr3:10183551
GRCh38:
Chr3:10141867
VHLN7SErythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Jan 15, 2020)
criteria provided, single submitterVCV001002447
82.
GRCh37:
Chr3:10183551
GRCh38:
Chr3:10141867
VHLN7IVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(Mar 22, 2019)
criteria provided, single submitterVCV000843835
83.
GRCh37:
Chr3:10183551
GRCh38:
Chr3:10141867
VHLN7TVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(Oct 11, 2018)
criteria provided, single submitterVCV000655972
84.
GRCh37:
Chr3:10183552
GRCh38:
Chr3:10141868
VHLN7KVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(Aug 20, 2020)
criteria provided, single submitterVCV000849658
85.
GRCh37:
Chr3:10183552
GRCh38:
Chr3:10141868
VHLnot specified, Von Hippel-Lindau syndrome, Erythrocytosis, familial, 2
Likely benign
(Nov 10, 2020)
criteria provided, multiple submitters, no conflictsVCV000514042
86.
GRCh37:
Chr3:10183552
GRCh38:
Chr3:10141868
VHLN7KHereditary cancer-predisposing syndrome, Von Hippel-Lindau syndrome, Erythrocytosis, familial, 2,
not provided
Uncertain significance
(Aug 4, 2020)
criteria provided, multiple submitters, no conflictsVCV000411973
87.
GRCh37:
Chr3:10183553
GRCh38:
Chr3:10141869
VHLW8RVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(May 15, 2017)
criteria provided, single submitterVCV000456575
88.
GRCh37:
Chr3:10183554
GRCh38:
Chr3:10141870
VHLW8LErythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Aug 21, 2019)
criteria provided, single submitterVCV000936341
89.
GRCh37:
Chr3:10183554
GRCh38:
Chr3:10141870
VHLW8*Von Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(Sep 28, 2016)
criteria provided, single submitterVCV000411960
90.
GRCh37:
Chr3:10183556
GRCh38:
Chr3:10141872
VHLD9HErythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Nov 20, 2018)
criteria provided, single submitterVCV000651779
91.
GRCh37:
Chr3:10183556
GRCh38:
Chr3:10141872
VHLD9NVon Hippel-Lindau syndrome, not provided, Erythrocytosis, familial, 2,
Von Hippel-Lindau syndrome
Uncertain significance
(Aug 25, 2021)
criteria provided, multiple submitters, no conflictsVCV000135953
92.
GRCh37:
Chr3:10183557
GRCh38:
Chr3:10141873
VHLD9AVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(Oct 9, 2019)
criteria provided, single submitterVCV000411971
93.
GRCh37:
Chr3:10183558
GRCh38:
Chr3:10141874
VHLD9EVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(Jan 28, 2019)
criteria provided, single submitterVCV000846969
94.
GRCh37:
Chr3:10183558
GRCh38:
Chr3:10141874
VHLErythrocytosis, familial, 2, Von Hippel-Lindau syndromeLikely benign
(Nov 27, 2020)
criteria provided, single submitterVCV000416992
95.
GRCh37:
Chr3:10183558
GRCh38:
Chr3:10141874
VHLD9EVon Hippel-Lindau syndrome, Erythrocytosis, familial, 2Uncertain significance
(Oct 23, 2020)
criteria provided, single submitterVCV000411975
96.
GRCh37:
Chr3:10183559
GRCh38:
Chr3:10141875
VHLE10QErythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Oct 18, 2020)
criteria provided, single submitterVCV001042098
97.
GRCh37:
Chr3:10183559
GRCh38:
Chr3:10141875
VHLE10*Von Hippel-Lindau syndrome, Erythrocytosis, familial, 2, Von Hippel-Lindau syndrome
Uncertain significance
(Jun 30, 2020)
criteria provided, multiple submitters, no conflictsVCV000548745
98.
GRCh37:
Chr3:10183559
GRCh38:
Chr3:10141875
VHLE10Knot provided, Von Hippel-Lindau syndrome, Von Hippel-Lindau syndrome,
Erythrocytosis, familial, 2, Hereditary cancer-predisposing syndrome
Uncertain significance
(Nov 1, 2020)
criteria provided, multiple submitters, no conflictsVCV000374982
99.
GRCh37:
Chr3:10183560
GRCh38:
Chr3:10141876
VHLE10GErythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Feb 3, 2020)
criteria provided, single submitterVCV001005487
100.
GRCh37:
Chr3:10183560
GRCh38:
Chr3:10141876
VHLE10VErythrocytosis, familial, 2, Von Hippel-Lindau syndromeUncertain significance
(Nov 14, 2019)
criteria provided, single submitterVCV000188098
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