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Items: 1 to 100 of 175

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
TMC1Deafness, autosomal recessive 7Pathogenic
(Dec 1, 2007)
no assertion criteria provided
2.
GRCh37:
Chr9:23524426-87359888
GliomaLikely pathogenic
(Jun 5, 2017)
no assertion criteria provided
3.
GRCh37:
Chr9:75136717
GRCh38:
Chr9:72521801
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveLikely benign
(Jun 14, 2016)
criteria provided, single submitter
4.
GRCh37:
Chr9:75136789
GRCh38:
Chr9:72521873
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveBenign
(Jun 14, 2016)
criteria provided, single submitter
5.
GRCh37:
Chr9:75192895
GRCh38:
Chr9:72577979
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
6.
GRCh37:
Chr9:75192916
GRCh38:
Chr9:72578000
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveLikely benign
(Jun 14, 2016)
criteria provided, single submitter
7.
GRCh37:
Chr9:75231337
GRCh38:
Chr9:72616421
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
8.
GRCh37:
Chr9:75231369
GRCh38:
Chr9:72616453
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
9.
GRCh37:
Chr9:75231370
GRCh38:
Chr9:72616454
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveBenign
(Jun 14, 2016)
criteria provided, single submitter
10.
GRCh37:
Chr9:75242908
GRCh38:
Chr9:72627992
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
11.
GRCh37:
Chr9:75263571
GRCh38:
Chr9:72648655
TMC1not specifiedUncertain significance
(Dec 31, 2013)
criteria provided, single submitter
12.
GRCh37:
Chr9:75263579
GRCh38:
Chr9:72648663
TMC1Deafness, autosomal recessive 7Pathogenic
(Feb 16, 2016)
no assertion criteria provided
13.
GRCh37:
Chr9:75303630
GRCh38:
Chr9:72688714
TMC1Nonsyndromic hearing loss and deafnessPathogenic
(Aug 8, 2013)
criteria provided, single submitter
14.
GRCh37:
Chr9:75303653
GRCh38:
Chr9:72688737
TMC1Nonsyndromic Hearing Loss, Recessive, Nonsyndromic Hearing Loss, Dominant, not specified
Benign
(Jun 14, 2016)
criteria provided, multiple submitters, no conflicts
15.
GRCh37:
Chr9:75309449
GRCh38:
Chr9:72694533
TMC1not providedUncertain significance
(Sep 4, 2018)
criteria provided, single submitter
16.
GRCh37:
Chr9:75309494
GRCh38:
Chr9:72694578
TMC1Nonsyndromic hearing loss and deafness, not provided, Deafness, autosomal recessive 7
Pathogenic
(Dec 9, 2014)
criteria provided, multiple submitters, no conflicts
17.
GRCh37:
Chr9:75309529
GRCh38:
Chr9:72694613
TMC1not specifiedLikely benign
(Jan 26, 2018)
criteria provided, single submitter
18.
GRCh37:
Chr9:75309535
GRCh38:
Chr9:72694619
TMC1not specifiedUncertain significance
(Jul 21, 2015)
criteria provided, single submitter
19.
GRCh37:
Chr9:75309539
GRCh38:
Chr9:72694623
TMC1not specifiedUncertain significance
(Apr 5, 2016)
criteria provided, single submitter
20.
GRCh37:
Chr9:75309609-75309613
GRCh38:
Chr9:72694693-72694697
TMC1Nonsyndromic hearing loss and deafnessPathogenic
(Nov 26, 2013)
criteria provided, single submitter
21.
GRCh37:
Chr9:75309623
GRCh38:
Chr9:72694707
TMC1Deafness, autosomal recessive 7Pathogenic
(Feb 16, 2016)
no assertion criteria provided
22.
GRCh37:
Chr9:75309631
GRCh38:
Chr9:72694715
TMC1Nonsyndromic hearing loss and deafness, Deafness, autosomal dominant 36, Deafness, autosomal recessive 7
Pathogenic/Likely pathogenic
(May 27, 2016)
criteria provided, multiple submitters, no conflicts
23.
GRCh37:
Chr9:75315429
GRCh38:
Chr9:72700513
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
24.
GRCh37:
Chr9:75315438
GRCh38:
Chr9:72700522
TMC1Nonsyndromic Hearing Loss, Recessive, not specified, Nonsyndromic Hearing Loss, Dominant
Benign/Likely benign
(Jun 14, 2016)
criteria provided, multiple submitters, no conflicts
25.
GRCh37:
Chr9:75315444-75315446
GRCh38:
Chr9:72700528-72700530
TMC1Nonsyndromic Hearing Loss, Recessive, Nonsyndromic Hearing Loss, Dominant, not specified
Benign/Likely benign
(Jun 14, 2016)
criteria provided, multiple submitters, no conflicts
26.
GRCh37:
Chr9:75315462
GRCh38:
Chr9:72700546
TMC1not providedUncertain significance
(May 3, 2016)
criteria provided, single submitter
27.
GRCh37:
Chr9:75315536
GRCh38:
Chr9:72700620
TMC1not specifiedUncertain significance
(Oct 7, 2010)
criteria provided, single submitter
28.
GRCh37:
Chr9:75355045
GRCh38:
Chr9:72740129
TMC1not providedUncertain significance
(May 14, 2018)
criteria provided, single submitter
29.
GRCh37:
Chr9:75355075
GRCh38:
Chr9:72740159
TMC1not specifiedUncertain significance
(Feb 1, 2011)
criteria provided, single submitter
30.
GRCh37:
Chr9:75355093
GRCh38:
Chr9:72740177
TMC1Nonsyndromic Hearing Loss, Recessive, Nonsyndromic Hearing Loss, Dominant, not specified
Benign/Likely benign
(Jun 14, 2016)
criteria provided, multiple submitters, no conflicts
31.
GRCh37:
Chr9:75355120
GRCh38:
Chr9:72740204
TMC1not specifiedUncertain significance
(Dec 11, 2017)
criteria provided, single submitter
32.
GRCh37:
Chr9:75357378
GRCh38:
Chr9:72742462
TMC1not specifiedUncertain significance
(May 16, 2017)
criteria provided, single submitter
33.
GRCh37:
Chr9:75357379
GRCh38:
Chr9:72742463
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
34.
GRCh37:
Chr9:75357389
GRCh38:
Chr9:72742473
TMC1not specifiedLikely benign
(Aug 31, 2016)
criteria provided, single submitter
35.
GRCh37:
Chr9:75357440
GRCh38:
Chr9:72742524
TMC1not providedUncertain significance
(Jul 27, 2015)
criteria provided, single submitter
36.
GRCh37:
Chr9:75366787
GRCh38:
Chr9:72751871
TMC1not specifiedUncertain significance
(May 6, 2013)
criteria provided, single submitter
37.
GRCh37:
Chr9:75366812
GRCh38:
Chr9:72751896
TMC1not providedLikely pathogenic
(Feb 5, 2019)
criteria provided, single submitter
38.
GRCh37:
Chr9:75366821-75366822
GRCh38:
Chr9:72751906
TMC1TMC1-Related DisordersUncertain significance
(Oct 16, 2018)
criteria provided, single submitter
39.
GRCh37:
Chr9:75366833
GRCh38:
Chr9:72751917
TMC1not providedUncertain significance
(May 31, 2016)
criteria provided, single submitter
40.
GRCh37:
Chr9:75366854
GRCh38:
Chr9:72751938
TMC1Deafness, autosomal dominant 36, Deafness, autosomal recessive 7Uncertain significance
(Feb 25, 2016)
no assertion criteria provided
41.
GRCh37:
Chr9:75366867
GRCh38:
Chr9:72751951
TMC1not specifiedUncertain significance
(Jun 30, 2016)
criteria provided, single submitter
42.
GRCh37:
Chr9:75369733
GRCh38:
Chr9:72754817
TMC1Nonsyndromic hearing loss and deafnessLikely pathogenic
(Mar 6, 2015)
criteria provided, single submitter
43.
GRCh37:
Chr9:75369743
GRCh38:
Chr9:72754827
TMC1not specifiedLikely benign
(May 10, 2016)
criteria provided, single submitter
44.
GRCh37:
Chr9:75369762
GRCh38:
Chr9:72754846
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
45.
GRCh37:
Chr9:75387317
GRCh38:
Chr9:72772401
TMC1not specifiedLikely benigncriteria provided, single submitter
46.
GRCh37:
Chr9:75387347
GRCh38:
Chr9:72772431
TMC1not specifiedLikely benign
(Feb 7, 2013)
criteria provided, single submitter
47.
GRCh37:
Chr9:75387364
GRCh38:
Chr9:72772448
TMC1not specifiedLikely benign
(Apr 5, 2013)
criteria provided, single submitter
48.
GRCh37:
Chr9:75387378
GRCh38:
Chr9:72772462
TMC1not specifiedUncertain significance
(Apr 15, 2011)
criteria provided, single submitter
49.
GRCh37:
Chr9:75387382
GRCh38:
Chr9:72772466
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, Recessive, not specified
Conflicting interpretations of pathogenicity
(Jun 14, 2016)
criteria provided, conflicting interpretations
50.
GRCh37:
Chr9:75387417
GRCh38:
Chr9:72772501
TMC1not providedUncertain significance
(Jul 9, 2018)
criteria provided, single submitter
51.
GRCh37:
Chr9:75387428
GRCh38:
Chr9:72772512
TMC1not specifiedUncertain significance
(Aug 26, 2011)
criteria provided, single submitter
52.
GRCh37:
Chr9:75387473
GRCh38:
Chr9:72772557
TMC1not specifiedUncertain significance
(Nov 12, 2015)
criteria provided, single submitter
53.
GRCh37:
Chr9:75403253
GRCh38:
Chr9:72788337
TMC1Deafness, autosomal recessive 7Pathogenic
(May 23, 2016)
criteria provided, single submitter
54.
GRCh37:
Chr9:75403280
GRCh38:
Chr9:72788364
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
55.
GRCh37:
Chr9:75403294
GRCh38:
Chr9:72788378
TMC1not provided, Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, Recessive
Uncertain significance
(Jun 14, 2016)
criteria provided, multiple submitters, no conflicts
56.
GRCh37:
Chr9:75403308
GRCh38:
Chr9:72788392
TMC1Deafness, autosomal dominant 36, Deafness, autosomal recessive 7Uncertain significance
(Feb 26, 2016)
no assertion criteria provided
57.
GRCh37:
Chr9:75403315
GRCh38:
Chr9:72788399
TMC1DeafnessPathogenic
(Sep 10, 2018)
no assertion criteria provided
58.
GRCh37:
Chr9:75403326
GRCh38:
Chr9:72788410
TMC1not providedUncertain significance
(Jun 7, 2016)
criteria provided, single submitter
59.
GRCh37:
Chr9:75403388
GRCh38:
Chr9:72788472
TMC1not specifiedUncertain significance
(Dec 19, 2014)
criteria provided, single submitter
60.
GRCh37:
Chr9:75403389
GRCh38:
Chr9:72788473
TMC1not specifiedLikely benign
(Nov 2, 2009)
no assertion criteria provided
61.
GRCh37:
Chr9:75403392
GRCh38:
Chr9:72788476
TMC1not specifiedUncertain significance
(Oct 5, 2013)
criteria provided, single submitter
62.
GRCh37:
Chr9:75404036
GRCh38:
Chr9:72789120
TMC1not specifiedUncertain significance
(Jan 28, 2017)
criteria provided, single submitter
63.
GRCh37:
Chr9:75404079
GRCh38:
Chr9:72789163
TMC1not specifiedLikely benign
(Sep 2, 2010)
criteria provided, single submitter
64.
GRCh37:
Chr9:75404080
GRCh38:
Chr9:72789164
TMC1not specifiedLikely benign
(Jan 25, 2018)
criteria provided, single submitter
65.
GRCh37:
Chr9:75404123
GRCh38:
Chr9:72789207
TMC1not provided, Deafness, autosomal recessive 7Conflicting interpretations of pathogenicity
(Apr 17, 2018)
criteria provided, conflicting interpretations
66.
GRCh37:
Chr9:75404150
GRCh38:
Chr9:72789234
TMC1not provided, Nonsyndromic hearing loss and deafnessConflicting interpretations of pathogenicity
(Nov 2, 2017)
criteria provided, conflicting interpretations
67.
GRCh37:
Chr9:75404152
GRCh38:
Chr9:72789236
TMC1Deafness, autosomal recessive 7Pathogenic
(Jul 5, 2018)
no assertion criteria provided
68.
GRCh37:
Chr9:75404174
GRCh38:
Chr9:72789258
TMC1Nonsyndromic hearing loss and deafness, not providedPathogenic
(Sep 5, 2013)
criteria provided, multiple submitters, no conflicts
69.
GRCh37:
Chr9:75404198
GRCh38:
Chr9:72789282
TMC1not specifiedUncertain significance
(Nov 12, 2015)
criteria provided, single submitter
70.
GRCh37:
Chr9:75404218
GRCh38:
Chr9:72789302
TMC1DeafnessPathogenic
(Sep 10, 2018)
no assertion criteria provided
71.
GRCh37:
Chr9:75404219
GRCh38:
Chr9:72789303
TMC1no interpretation for the single variantno interpretation for the single variant
72.
GRCh37:
Chr9:75404227-75404228
GRCh38:
Chr9:72789311-72789312
TMC1Deafness, autosomal recessive 7Pathogenic
(Jul 5, 2018)
no assertion criteria provided
73.
GRCh37:
Chr9:75404235
GRCh38:
Chr9:72789319
TMC1DeafnessPathogenic
(Sep 10, 2018)
no assertion criteria provided
74.
GRCh37:
Chr9:75404238
GRCh38:
Chr9:72789322
TMC1not specifiedUncertain significance
(Feb 7, 2013)
criteria provided, single submitter
75.
GRCh37:
Chr9:75406794
GRCh38:
Chr9:72791878
TMC1not specifiedLikely benign
(May 24, 2013)
criteria provided, single submitter
76.
GRCh37:
Chr9:75406810
GRCh38:
Chr9:72791894
TMC1not specifiedLikely benign
(Sep 7, 2013)
criteria provided, single submitter
77.
GRCh37:
Chr9:75406813
GRCh38:
Chr9:72791897
TMC1Nonsyndromic hearing loss and deafness, not providedPathogenic
(Oct 12, 2015)
criteria provided, multiple submitters, no conflicts
78.
GRCh37:
Chr9:75406830
GRCh38:
Chr9:72791914
TMC1Deafness, autosomal dominant 36Pathogenic
(Jan 1, 2014)
no assertion criteria provided
79.
GRCh37:
Chr9:75406836
GRCh38:
Chr9:72791920
TMC1Deafness, autosomal recessive 7Pathogenic
(Jul 1, 2018)
no assertion criteria provided
80.
GRCh37:
Chr9:75406840
GRCh38:
Chr9:72791924
TMC1not specifiedLikely benign
(Apr 30, 2012)
criteria provided, multiple submitters, no conflicts
81.
GRCh37:
Chr9:75406842
GRCh38:
Chr9:72791926
TMC1not specifiedUncertain significance
(Oct 4, 2016)
criteria provided, single submitter
82.
GRCh37:
Chr9:75406910
GRCh38:
Chr9:72791994
TMC1Nonsyndromic hearing loss and deafness, Deafness, autosomal recessive 7, not provided
Conflicting interpretations of pathogenicity
(Jul 9, 2014)
criteria provided, conflicting interpretations
83.
GRCh37:
Chr9:75406946
GRCh38:
Chr9:72792030
TMC1not specifiedUncertain significance
(Aug 1, 2011)
criteria provided, single submitter
84.
GRCh37:
Chr9:75406985
GRCh38:
Chr9:72792069
TMC1not specifiedUncertain significance
(Oct 19, 2014)
criteria provided, single submitter
85.
GRCh37:
Chr9:75407151
GRCh38:
Chr9:72792235
TMC1not providedUncertain significance
(May 14, 2018)
criteria provided, single submitter
86.
GRCh37:
Chr9:75407159
GRCh38:
Chr9:72792243
TMC1Nonsyndromic Hearing Loss, Recessive, not specified, Nonsyndromic Hearing Loss, Dominant
Benign/Likely benign
(Jun 14, 2016)
criteria provided, multiple submitters, no conflicts
87.
GRCh37:
Chr9:75407234
GRCh38:
Chr9:72792318
TMC1Deafness, autosomal recessive 7Pathogenic
(Jun 4, 2016)
no assertion criteria provided
88.
GRCh37:
Chr9:75407234
GRCh38:
Chr9:72792318
TMC1not specifiedUncertain significance
(Sep 10, 2013)
criteria provided, single submitter
89.
GRCh37:
Chr9:75407236
GRCh38:
Chr9:72792320
TMC1not providedPathogenic
(May 11, 2018)
criteria provided, single submitter
90.
GRCh37:
Chr9:75407245
GRCh38:
Chr9:72792329
TMC1Deafness, autosomal recessive 7Pathogenic
(Dec 1, 2007)
no assertion criteria provided
91.
GRCh37:
Chr9:75407276
GRCh38:
Chr9:72792360
TMC1not specifiedLikely benign
(May 17, 2015)
criteria provided, single submitter
92.
GRCh37:
Chr9:75420284
GRCh38:
Chr9:72805368
TMC1not specified, Deafness, autosomal recessive 7, Deafness, autosomal dominant 36
Uncertain significance
(May 3, 2015)
criteria provided, multiple submitters, no conflicts
93.
GRCh37:
Chr9:75420294
GRCh38:
Chr9:72805378
TMC1not specifiedLikely benign
(Jun 2, 2016)
criteria provided, single submitter
94.
GRCh37:
Chr9:75420315
GRCh38:
Chr9:72805399
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
95.
GRCh37:
Chr9:75420333
GRCh38:
Chr9:72805417
TMC1not specifiedLikely benign
(Oct 20, 2009)
criteria provided, single submitter
96.
GRCh37:
Chr9:75420339
GRCh38:
Chr9:72805423
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
97.
GRCh37:
Chr9:75420340
GRCh38:
Chr9:72805424
TMC1Nonsyndromic Hearing Loss, Dominant, Nonsyndromic Hearing Loss, RecessiveUncertain significance
(Jun 14, 2016)
criteria provided, single submitter
98.
GRCh37:
Chr9:75420353
GRCh38:
Chr9:72805437
TMC1not providedUncertain significance
(May 3, 2016)
criteria provided, single submitter
99.
GRCh37:
Chr9:75420407
GRCh38:
Chr9:72805491
TMC1Nonsyndromic hearing loss and deafnessPathogenic
(Dec 22, 2016)
criteria provided, single submitter
100.
GRCh37:
Chr9:75420408
GRCh38:
Chr9:72805492
TMC1Nonsyndromic hearing loss and deafnessPathogenic
(Feb 12, 2015)
criteria provided, single submitter
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