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Items: 1 to 100 of 793

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review statusAccession
1.
GRCh37:
Chr15:73612237
GRCh38:
Chr15:73319896
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000885564
2.
GRCh37:
Chr15:73612241
GRCh38:
Chr15:73319900
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000885565
3.
GRCh37:
Chr15:73612377
GRCh38:
Chr15:73320036
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000885566
4.
GRCh37:
Chr15:73612429
GRCh38:
Chr15:73320088
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000885567
5.
GRCh37:
Chr15:73612468
GRCh38:
Chr15:73320127
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000885568
6.
GRCh37:
Chr15:73612581
GRCh38:
Chr15:73320240
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000885569
7.
GRCh37:
Chr15:73612812
GRCh38:
Chr15:73320471
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000886589
8.
GRCh37:
Chr15:73612833
GRCh38:
Chr15:73320492
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000886590
9.
GRCh37:
Chr15:73612988
GRCh38:
Chr15:73320647
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000886591
10.
GRCh37:
Chr15:73613163
GRCh38:
Chr15:73320822
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000886592
11.
GRCh37:
Chr15:73613224
GRCh38:
Chr15:73320883
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000886593
12.
GRCh37:
Chr15:73613332
GRCh38:
Chr15:73320991
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000886594
13.
GRCh37:
Chr15:73613340
GRCh38:
Chr15:73320999
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000886595
14.
GRCh37:
Chr15:73613617
GRCh38:
Chr15:73321276
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 15, 2018)
criteria provided, single submitterVCV000886596
15.
GRCh37:
Chr15:73613625
GRCh38:
Chr15:73321284
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000887841
16.
GRCh37:
Chr15:73613650
GRCh38:
Chr15:73321309
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000887842
17.
GRCh37:
Chr15:73613682
GRCh38:
Chr15:73321341
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000887843
18.
GRCh37:
Chr15:73613737
GRCh38:
Chr15:73321396
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000887844
19.
GRCh37:
Chr15:73613842
GRCh38:
Chr15:73321501
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000887845
20.
GRCh37:
Chr15:73613921
GRCh38:
Chr15:73321580
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000887846
21.
GRCh37:
Chr15:73613975
GRCh38:
Chr15:73321634
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000887847
22.
GRCh37:
Chr15:73613978
GRCh38:
Chr15:73321637
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000887848
23.
GRCh37:
Chr15:73614055
GRCh38:
Chr15:73321714
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000884687
24.
GRCh37:
Chr15:73614114
GRCh38:
Chr15:73321773
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000884688
25.
GRCh37:
Chr15:73614188
GRCh38:
Chr15:73321847
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000884689
26.
GRCh37:
Chr15:73614230
GRCh38:
Chr15:73321889
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000884690
27.
GRCh37:
Chr15:73614408
GRCh38:
Chr15:73322067
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000884691
28.
GRCh37:
Chr15:73614654
GRCh38:
Chr15:73322313
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000884692
29.
GRCh37:
Chr15:73614695
GRCh38:
Chr15:73322354
HCN4Sick sinus syndrome 2, autosomal dominantBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000884693
30.
GRCh37:
Chr15:73614703-73614704
GRCh38:
Chr15:73322362-73322363
HCN4not providedBenign
(Jun 15, 2018)
criteria provided, single submitterVCV001288341
31.
GRCh37:
Chr15:73614718
GRCh38:
Chr15:73322377
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000884694
32.
GRCh37:
Chr15:73614778
GRCh38:
Chr15:73322437
HCN4Sick sinus syndrome 2, autosomal dominantUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000885635
33.
GRCh37:
Chr15:73614814
GRCh38:
Chr15:73322473
HCN4not providedUncertain significance
(Aug 30, 2016)
criteria provided, single submitterVCV000289951
34.
GRCh37:
Chr15:73614820
GRCh38:
Chr15:73322479
HCN4not providedLikely benign
(Sep 25, 2019)
criteria provided, single submitterVCV001210474
35.
GRCh37:
Chr15:73614825
GRCh38:
Chr15:73322484
HCN4Brugada syndrome 8Uncertain significance
(Feb 26, 2019)
criteria provided, single submitterVCV000837958
36.
GRCh37:
Chr15:73614829
GRCh38:
Chr15:73322488
HCN4N1202SBrugada syndrome 8Uncertain significance
(Aug 26, 2020)
criteria provided, single submitterVCV000538092
37.
GRCh37:
Chr15:73614834
GRCh38:
Chr15:73322493
HCN4Brugada syndrome 8Likely benign
(Jan 23, 2020)
criteria provided, single submitterVCV000799842
38.
GRCh37:
Chr15:73614834-73614835
GRCh38:
Chr15:73322493-73322494
HCN4P1200LBrugada syndrome 8Uncertain significance
(Apr 2, 2018)
criteria provided, single submitterVCV000575303
39.
GRCh37:
Chr15:73614834
GRCh38:
Chr15:73322493
HCN4Sick sinus syndrome 2, autosomal dominant, Brugada syndrome 8, not specified,
not provided, Cardiovascular phenotype
Benign
(Dec 8, 2020)
criteria provided, multiple submitters, no conflictsVCV000095285
40.
GRCh37:
Chr15:73614837
GRCh38:
Chr15:73322496
HCN4Brugada syndrome 8Likely benign
(Nov 2, 2019)
criteria provided, single submitterVCV001141786
41.
GRCh37:
Chr15:73614838
GRCh38:
Chr15:73322497
HCN4L1199QBrugada syndrome 8, not providedUncertain significance
(Aug 21, 2017)
criteria provided, multiple submitters, no conflictsVCV000502460
42.
GRCh37:
Chr15:73614847
GRCh38:
Chr15:73322506
HCN4R1196HBrugada syndrome 8, Cardiovascular phenotype, not specified,
not provided
Benign
(Dec 3, 2020)
criteria provided, multiple submitters, no conflictsVCV000198820
43.
GRCh37:
Chr15:73614848
GRCh38:
Chr15:73322507
HCN4R1196CBrugada syndrome 8Uncertain significance
(Aug 23, 2019)
criteria provided, single submitterVCV000538090
44.
GRCh37:
Chr15:73614852
GRCh38:
Chr15:73322511
HCN4Brugada syndrome 8, not providedUncertain significance
(Oct 15, 2020)
criteria provided, multiple submitters, no conflictsVCV000489266
45.
GRCh37:
Chr15:73614855
GRCh38:
Chr15:73322514
HCN4Brugada syndrome 8Likely benign
(Feb 19, 2020)
criteria provided, single submitterVCV001110861
46.
GRCh37:
Chr15:73614857
GRCh38:
Chr15:73322516
HCN4E1193QBrugada syndrome 8, not provided, Cardiovascular phenotype
Conflicting interpretations of pathogenicity
(Mar 30, 2021)
criteria provided, conflicting interpretationsVCV000191449
47.
GRCh37:
Chr15:73614859
GRCh38:
Chr15:73322518
HCN4P1192LBrugada syndrome 8Uncertain significance
(Oct 24, 2018)
criteria provided, single submitterVCV000579946
48.
GRCh37:
Chr15:73614866
GRCh38:
Chr15:73322525
HCN4A1190TBrugada syndrome 8Uncertain significance
(Sep 12, 2017)
criteria provided, single submitterVCV000404135
49.
GRCh37:
Chr15:73614893
GRCh38:
Chr15:73322552
HCN4T1181PBrugada syndrome 8Uncertain significance
(Aug 14, 2020)
criteria provided, single submitterVCV000941815
50.
GRCh37:
Chr15:73614897-73614898
GRCh38:
Chr15:73322556-73322557
HCN4L1180fsnot providedUncertain significance
(Jul 16, 2019)
criteria provided, single submitterVCV001307186
51.
GRCh37:
Chr15:73614901
GRCh38:
Chr15:73322560
HCN4P1178LBrugada syndrome 8Uncertain significance
(Sep 30, 2020)
criteria provided, single submitterVCV001040816
52.
GRCh37:
Chr15:73614903
GRCh38:
Chr15:73322562
HCN4Brugada syndrome 8Likely benign
(Jan 13, 2019)
criteria provided, single submitterVCV000701673
53.
GRCh37:
Chr15:73614903
GRCh38:
Chr15:73322562
HCN4Brugada syndrome 8, not specified, not provided
Likely benign
(Jun 27, 2020)
criteria provided, multiple submitters, no conflictsVCV000382170
54.
GRCh37:
Chr15:73614908
GRCh38:
Chr15:73322567
HCN4G1176RBrugada syndrome 8Uncertain significance
(Sep 27, 2017)
criteria provided, single submitterVCV000404126
55.
GRCh37:
Chr15:73614922
GRCh38:
Chr15:73322581
HCN4R1171Inot providedUncertain significance
(Mar 26, 2014)
criteria provided, single submitterVCV000190790
56.
GRCh37:
Chr15:73614929-73614932
GRCh38:
Chr15:73322588-73322591
HCN4F1168fsSinus node disease, Brugada syndrome 8, not provided
Uncertain significance
(Oct 19, 2020)
criteria provided, multiple submitters, no conflictsVCV000191377
57.
GRCh37:
Chr15:73614931
GRCh38:
Chr15:73322590
HCN4F1168SBrugada syndrome 8Uncertain significance
(Dec 22, 2019)
criteria provided, single submitterVCV000835426
58.
GRCh37:
Chr15:73614933
GRCh38:
Chr15:73322592
HCN4L1167FBrugada syndrome 8Uncertain significance
(Jan 24, 2020)
criteria provided, single submitterVCV001063007
59.
GRCh37:
Chr15:73614934-73614937
GRCh38:
Chr15:73322593-73322596
HCN4S1166fsnot specified, not provided, Brugada syndrome 8
Uncertain significance
(Sep 24, 2020)
criteria provided, multiple submitters, no conflictsVCV000190785
60.
GRCh37:
Chr15:73614944
GRCh38:
Chr15:73322603
HCN4P1164Snot providedUncertain significanceno assertion criteria providedVCV001284374
61.
GRCh37:
Chr15:73614944
GRCh38:
Chr15:73322603
HCN4P1164ABrugada syndrome 8Uncertain significance
(Oct 4, 2020)
criteria provided, single submitterVCV000849884
62.
GRCh37:
Chr15:73614946
GRCh38:
Chr15:73322605
HCN4P1163Hnot provided, Brugada syndrome 8Uncertain significance
(Oct 18, 2021)
criteria provided, multiple submitters, no conflictsVCV000404127
63.
GRCh37:
Chr15:73614947
GRCh38:
Chr15:73322606
HCN4P1163TBrugada syndrome 8, Cardiovascular phenotypeUncertain significance
(Jul 15, 2020)
criteria provided, multiple submitters, no conflictsVCV000519345
64.
GRCh37:
Chr15:73614966
GRCh38:
Chr15:73322625
HCN4not specified, Brugada syndrome 8Likely benign
(Mar 4, 2020)
criteria provided, multiple submitters, no conflictsVCV000383673
65.
GRCh37:
Chr15:73614973
GRCh38:
Chr15:73322632
HCN4R1154QBrugada syndrome 8, not providedUncertain significance
(Jan 31, 2020)
criteria provided, multiple submitters, no conflictsVCV000191450
66.
GRCh37:
Chr15:73614974
GRCh38:
Chr15:73322633
HCN4R1154Wnot providedUncertain significance
(May 6, 2021)
criteria provided, single submitterVCV001201442
67.
GRCh37:
Chr15:73614982
GRCh38:
Chr15:73322641
HCN4T1151IBrugada syndrome 8Uncertain significance
(Dec 5, 2019)
criteria provided, single submitterVCV000849472
68.
GRCh37:
Chr15:73614986
GRCh38:
Chr15:73322645
HCN4V1150Inot providedUncertain significance
(Feb 15, 2018)
criteria provided, multiple submitters, no conflictsVCV000234777
69.
GRCh37:
Chr15:73614987
GRCh38:
Chr15:73322646
HCN4Brugada syndrome 8Likely benign
(Sep 24, 2020)
criteria provided, single submitterVCV001136931
70.
GRCh37:
Chr15:73614987-73614988
GRCh38:
Chr15:73322646-73322647
HCN4H1149LBrugada syndrome 8Uncertain significance
(May 19, 2019)
criteria provided, single submitterVCV000945800
71.
GRCh37:
Chr15:73614996
GRCh38:
Chr15:73322655
HCN4Brugada syndrome 8Uncertain significance
(Aug 6, 2020)
criteria provided, single submitterVCV001007282
72.
GRCh37:
Chr15:73615001
GRCh38:
Chr15:73322660
HCN4I1145Vnot providedUncertain significance
(May 6, 2019)
criteria provided, single submitterVCV001305548
73.
GRCh37:
Chr15:73615006
GRCh38:
Chr15:73322665
HCN4G1143VBrugada syndrome 8Uncertain significance
(Jun 20, 2017)
criteria provided, single submitterVCV000470670
74.
GRCh37:
Chr15:73615017
GRCh38:
Chr15:73322676
HCN4Brugada syndrome 8Likely benign
(Aug 26, 2020)
criteria provided, single submitterVCV001158710
75.
GRCh37:
Chr15:73615020
GRCh38:
Chr15:73322679
HCN4R1140fsCardiovascular phenotype, Brugada syndrome 8Uncertain significance
(Dec 19, 2019)
criteria provided, multiple submitters, no conflictsVCV000518849
76.
GRCh37:
Chr15:73615022
GRCh38:
Chr15:73322681
HCN4P1138ACardiovascular phenotype, Brugada syndrome 8Uncertain significance
(Aug 20, 2016)
criteria provided, multiple submitters, no conflictsVCV000404130
77.
GRCh37:
Chr15:73615023
GRCh38:
Chr15:73322682
HCN4Brugada syndrome 8, not providedLikely benign
(Aug 13, 2018)
criteria provided, single submitterVCV000765308
78.
GRCh37:
Chr15:73615025
GRCh38:
Chr15:73322684
HCN4P1137Snot provided, Brugada syndrome 8Uncertain significance
(Aug 9, 2019)
criteria provided, multiple submitters, no conflictsVCV000580597
79.
GRCh37:
Chr15:73615027
GRCh38:
Chr15:73322686
HCN4G1136VBrugada syndrome 8Uncertain significance
(Jun 27, 2017)
criteria provided, single submitterVCV000470669
80.
GRCh37:
Chr15:73615028
GRCh38:
Chr15:73322687
HCN4G1136SBrugada syndrome 8Uncertain significance
(Nov 12, 2019)
criteria provided, single submitterVCV000538091
81.
GRCh37:
Chr15:73615029
GRCh38:
Chr15:73322688
HCN4Brugada syndrome 8Likely benign
(Sep 11, 2020)
criteria provided, single submitterVCV000470668
82.
GRCh37:
Chr15:73615033
GRCh38:
Chr15:73322692
HCN4G1134DBrugada syndrome 8Uncertain significance
(Jul 9, 2020)
criteria provided, single submitterVCV001058101
83.
GRCh37:
Chr15:73615037
GRCh38:
Chr15:73322696
HCN4G1133RBrugada syndrome 8Uncertain significance
(Feb 6, 2020)
criteria provided, single submitterVCV000945339
84.
GRCh37:
Chr15:73615037
GRCh38:
Chr15:73322696
HCN4G1133RBrugada syndrome 8Uncertain significance
(Oct 28, 2020)
criteria provided, single submitterVCV000859517
85.
GRCh37:
Chr15:73615038
GRCh38:
Chr15:73322697
HCN4not provided, Brugada syndrome 8, Cardiovascular phenotype
Likely benign
(Oct 9, 2020)
criteria provided, multiple submitters, no conflictsVCV000519231
86.
GRCh37:
Chr15:73615046
GRCh38:
Chr15:73322705
HCN4G1130Rnot specified, Brugada syndrome 8Uncertain significance
(Apr 18, 2018)
criteria provided, multiple submitters, no conflictsVCV000447481
87.
GRCh37:
Chr15:73615048
GRCh38:
Chr15:73322707
HCN4S1129NBrugada syndrome 8Uncertain significance
(Oct 29, 2020)
criteria provided, single submitterVCV001018575
88.
GRCh37:
Chr15:73615051
GRCh38:
Chr15:73322710
HCN4G1128Vnot providedUncertain significance
(Feb 17, 2014)
criteria provided, single submitterVCV000167168
89.
GRCh37:
Chr15:73615052
GRCh38:
Chr15:73322711
HCN4G1128SCardiovascular phenotype, not provided, Brugada syndrome 8
Uncertain significance
(Nov 21, 2019)
criteria provided, multiple submitters, no conflictsVCV000518776
90.
GRCh37:
Chr15:73615055
GRCh38:
Chr15:73322714
HCN4G1127RBrugada syndrome 8, not providedUncertain significance
(Dec 10, 2019)
criteria provided, multiple submitters, no conflictsVCV000470667
91.
GRCh37:
Chr15:73615056
GRCh38:
Chr15:73322715
HCN4S1126Rnot providedUncertain significance
(Nov 8, 2019)
criteria provided, single submitterVCV001310223
92.
GRCh37:
Chr15:73615056
GRCh38:
Chr15:73322715
HCN4not providedLikely benign
(Dec 26, 2019)
criteria provided, single submitterVCV001226847
93.
GRCh37:
Chr15:73615063
GRCh38:
Chr15:73322722
HCN4G1124DBrugada syndrome 8Uncertain significance
(Feb 18, 2020)
criteria provided, single submitterVCV001046643
94.
GRCh37:
Chr15:73615071
GRCh38:
Chr15:73322730
HCN4R1121Snot providedUncertain significance
(May 27, 2015)
criteria provided, single submitterVCV000198824
95.
GRCh37:
Chr15:73615080
GRCh38:
Chr15:73322739
HCN4Brugada syndrome 8Likely benign
(Mar 26, 2017)
criteria provided, single submitterVCV000470666
96.
GRCh37:
Chr15:73615081
GRCh38:
Chr15:73322740
HCN4L1118PBrugada syndrome 8Uncertain significance
(Oct 12, 2017)
criteria provided, single submitterVCV000538089
97.
GRCh37:
Chr15:73615083
GRCh38:
Chr15:73322742
HCN4Brugada syndrome 8, not providedLikely benign
(Dec 4, 2020)
criteria provided, multiple submitters, no conflictsVCV000538098
98.
GRCh37:
Chr15:73615084
GRCh38:
Chr15:73322743
HCN4P1117LCardiovascular phenotype, Brugada syndrome 8, Sick sinus syndrome 2, autosomal dominant,
not specified, not provided
Benign/Likely benign
(Nov 27, 2020)
criteria provided, multiple submitters, no conflictsVCV000198826
99.
GRCh37:
Chr15:73615097
GRCh38:
Chr15:73322756
HCN4M1113VCardiomyopathy, Sick sinus syndrome 2, autosomal dominant, Brugada syndrome 8,
not specified, Cardiovascular phenotype
Benign
(Dec 8, 2020)
criteria provided, multiple submitters, no conflictsVCV000137543
100.
GRCh37:
Chr15:73615107
GRCh38:
Chr15:73322766
HCN4not specifiedLikely benign
(Feb 22, 2016)
criteria provided, single submitterVCV000384049
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