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Items: 1 to 100 of 129

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr6:133802621-133802622
GRCh38:
Chr6:133481483-133481484
EYA4S277fs, S308fs, S331fs, S337fs, S283fsAutosomal dominant nonsyndromic hearing loss 10Pathogenic
(Feb 28, 2023)
criteria provided, single submitter
2.
GRCh37:
Chr6:133834143
GRCh38:
Chr6:133513005
EYA4, TARIDE436*, E442*, E467*, E490*, E496*Autosomal dominant nonsyndromic hearing loss 10Likely pathogenic
(May 22, 2022)
criteria provided, single submitter
3.
GRCh37:
Chr6:133849847
GRCh38:
Chr6:133528709
TARID, EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J
Likely benign
(Oct 24, 2022)
criteria provided, multiple submitters, no conflicts
4.
GRCh37:
Chr6:133844181
GRCh38:
Chr6:133523043
TARID, EYA4Dilated cardiomyopathy 1J, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Benign/Likely benign
(Sep 25, 2021)
criteria provided, multiple submitters, no conflicts
5.
GRCh37:
Chr6:133834169
GRCh38:
Chr6:133513031
EYA4, TARIDCardiovascular phenotype, Dilated cardiomyopathy 1J, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Likely benign
(Sep 20, 2022)
criteria provided, multiple submitters, no conflicts
6.
GRCh37:
Chr6:133802697
GRCh38:
Chr6:133481559
EYA4R308Q, R356Q, R302Q, R362Q, R333QDilated cardiomyopathy 1J, not provided, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Jul 18, 2022)
criteria provided, multiple submitters, no conflicts
7.
GRCh37:
Chr6:133783864
GRCh38:
Chr6:133462726
EYA4P229L, P175L, P206LDilated cardiomyopathy 1J, not provided, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Nov 3, 2022)
criteria provided, multiple submitters, no conflicts
8.
GRCh37:
Chr6:133769253
GRCh38:
Chr6:133448115
EYA4E71DAutosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J, Dilated cardiomyopathy 1J,
Cardiovascular phenotype
Conflicting interpretations of pathogenicity
(Sep 14, 2022)
criteria provided, conflicting interpretations
9.
GRCh37:
Chr6:133846375
GRCh38:
Chr6:133525237
EYA4, TARIDE614Q, E560Q, E585Q, E608QAutosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J, Dilated cardiomyopathy 1J
Uncertain significance
(Sep 1, 2022)
criteria provided, multiple submitters, no conflicts
10.
GRCh37:
Chr6:133802676-133802677
GRCh38:
Chr6:133481538-133481539
EYA4R298fs, R304fs, R329fs, R352fs, R358fsAutosomal dominant nonsyndromic hearing loss 10Pathogenic
(Jul 15, 2007)
no assertion criteria provided
11.
GRCh37:
Chr6:133802655-133802656
GRCh38:
Chr6:133481517-133481518
EYA4T289fs, T295fs, T320fs, T343fs, T349fsAutosomal dominant nonsyndromic hearing loss 10Pathogenic
(Apr 1, 2005)
no assertion criteria provided
12.
GRCh37:
Chr6:133852742
GRCh38:
Chr6:133531604
TARID, EYA4not provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Likely benign
(Aug 9, 2021)
criteria provided, multiple submitters, no conflicts
13.
GRCh37:
Chr6:133789723
GRCh38:
Chr6:133468585
EYA4A221V, A252V, A275VDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, not provided,
Dilated cardiomyopathy 1J
Uncertain significance
(Oct 12, 2021)
criteria provided, multiple submitters, no conflicts
14.
GRCh37:
Chr6:133804216
GRCh38:
Chr6:133483078
EYA4S331*, S337*, S362*, S385*, S391*Autosomal dominant nonsyndromic hearing loss 10Pathogenic
(Jul 22, 2021)
criteria provided, single submitter
15.
GRCh37:
Chr6:133777802
GRCh38:
Chr6:133456664
EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J,
not specified
Benign/Likely benign
(Oct 31, 2022)
criteria provided, multiple submitters, no conflicts
16.
GRCh37:
Chr6:133785998
GRCh38:
Chr6:133464860
EYA4Autosomal dominant nonsyndromic hearing loss 10Pathogenicno assertion criteria provided
17.
GRCh37:
Chr6:133785998
GRCh38:
Chr6:133464860
EYA4Autosomal dominant nonsyndromic hearing loss 10Pathogenicno assertion criteria provided
18.
GRCh37:
Chr6:133789863
GRCh38:
Chr6:133468725
EYA4Q268*, Q299*, Q322*Autosomal dominant nonsyndromic hearing loss 10Pathogenic
(Jul 1, 2021)
no assertion criteria provided
19.
GRCh37:
Chr6:133595950
GRCh38:
Chr6:133274812
EYA4S11LDilated cardiomyopathy 1J, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Aug 31, 2021)
criteria provided, multiple submitters, no conflicts
20.
GRCh37:
Chr6:133783507
GRCh38:
Chr6:133462369
EYA4Q104*, Q135*, Q158*Autosomal dominant nonsyndromic hearing loss 10Likely pathogenic
(Jan 1, 2019)
criteria provided, single submitter
21.
GRCh37:
Chr6:133804243
GRCh38:
Chr6:133483105
EYA4K340R, K394R, K400R, K346R, K371RAutosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1JUncertain significance
(Jan 13, 2018)
criteria provided, single submitter
22.
GRCh37:
Chr6:133802750
GRCh38:
Chr6:133481612
EYA4Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1JConflicting interpretations of pathogenicity
(Mar 8, 2022)
criteria provided, conflicting interpretations
23.
GRCh37:
Chr6:133777760
GRCh38:
Chr6:133456622
EYA4G115A, G92AAutosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1JUncertain significance
(Jan 13, 2018)
criteria provided, single submitter
24.
GRCh37:
Chr6:133853169
GRCh38:
Chr6:133532031
TARID, EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Jul 19, 2021)
criteria provided, multiple submitters, no conflicts
25.
GRCh37:
Chr6:133853154
GRCh38:
Chr6:133532016
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 12, 2018)
criteria provided, single submitter
26.
GRCh37:
Chr6:133853103
GRCh38:
Chr6:133531965
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
27.
GRCh37:
Chr6:133851543
GRCh38:
Chr6:133530405
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 12, 2018)
criteria provided, single submitter
28.
GRCh37:
Chr6:133850576
GRCh38:
Chr6:133529438
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 12, 2018)
criteria provided, single submitter
29.
GRCh37:
Chr6:133850509
GRCh38:
Chr6:133529371
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Apr 27, 2017)
criteria provided, single submitter
30.
GRCh37:
Chr6:133562709
GRCh38:
Chr6:133241571
EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Benign/Likely benign
(Jan 13, 2018)
criteria provided, single submitter
31.
GRCh37:
Chr6:133853075
GRCh38:
Chr6:133531937
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 12, 2018)
criteria provided, single submitter
32.
GRCh37:
Chr6:133853064
GRCh38:
Chr6:133531926
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Apr 27, 2017)
criteria provided, single submitter
33.
GRCh37:
Chr6:133851494
GRCh38:
Chr6:133530356
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Oct 12, 2021)
criteria provided, multiple submitters, no conflicts
34.
GRCh37:
Chr6:133851475
GRCh38:
Chr6:133530337
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Dec 20, 2021)
criteria provided, multiple submitters, no conflicts
35.
GRCh37:
Chr6:133851427
GRCh38:
Chr6:133530289
EYA4, TARIDnot provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Benign/Likely benign
(Sep 7, 2021)
criteria provided, multiple submitters, no conflicts
36.
GRCh37:
Chr6:133850322
GRCh38:
Chr6:133529184
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 12, 2018)
criteria provided, single submitter
37.
GRCh37:
Chr6:133850290
GRCh38:
Chr6:133529152
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
38.
GRCh37:
Chr6:133850251
GRCh38:
Chr6:133529113
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Apr 27, 2017)
criteria provided, single submitter
39.
GRCh37:
Chr6:133852861
GRCh38:
Chr6:133531723
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Benign/Likely benign
(Feb 23, 2022)
criteria provided, multiple submitters, no conflicts
40.
GRCh37:
Chr6:133852628
GRCh38:
Chr6:133531490
EYA4, TARIDnot provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Benign/Likely benign
(May 13, 2021)
criteria provided, multiple submitters, no conflicts
41.
GRCh37:
Chr6:133851992
GRCh38:
Chr6:133530854
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Jul 28, 2021)
criteria provided, multiple submitters, no conflicts
42.
GRCh37:
Chr6:133851987
GRCh38:
Chr6:133530849
EYA4, TARIDnot provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Conflicting interpretations of pathogenicity
(Aug 25, 2021)
criteria provided, conflicting interpretations
43.
GRCh37:
Chr6:133851886
GRCh38:
Chr6:133530748
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Sep 20, 2021)
criteria provided, multiple submitters, no conflicts
44.
GRCh37:
Chr6:133851383
GRCh38:
Chr6:133530245
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Apr 27, 2017)
criteria provided, single submitter
45.
GRCh37:
Chr6:133851306
GRCh38:
Chr6:133530168
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 12, 2018)
criteria provided, single submitter
46.
GRCh37:
Chr6:133850208
GRCh38:
Chr6:133529070
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
47.
GRCh37:
Chr6:133850165
GRCh38:
Chr6:133529027
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
48.
GRCh37:
Chr6:133849958
GRCh38:
Chr6:133528820
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
49.
GRCh37:
Chr6:133562627
GRCh38:
Chr6:133241489
EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Benign/Likely benign
(Jan 12, 2018)
criteria provided, single submitter
50.
GRCh37:
Chr6:133851289
GRCh38:
Chr6:133530151
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
51.
GRCh37:
Chr6:133850699
GRCh38:
Chr6:133529561
EYA4, TARIDAutosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1JUncertain significance
(Jan 12, 2018)
criteria provided, single submitter
52.
GRCh37:
Chr6:133850675
GRCh38:
Chr6:133529537
EYA4, TARIDDilated cardiomyopathy 1J, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10,
Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Jul 9, 2021)
criteria provided, multiple submitters, no conflicts
53.
GRCh37:
Chr6:133783458
GRCh38:
Chr6:133462320
EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Conflicting interpretations of pathogenicity
(Nov 26, 2021)
criteria provided, conflicting interpretations
54.
GRCh37:
Chr6:133562508
GRCh38:
Chr6:133241370
EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Benign/Likely benign
(Jan 13, 2018)
criteria provided, single submitter
55.
GRCh37:
Chr6:133852382
GRCh38:
Chr6:133531244
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 12, 2018)
criteria provided, single submitter
56.
GRCh37:
Chr6:133852320
GRCh38:
Chr6:133531182
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Feb 16, 2018)
criteria provided, single submitter
57.
GRCh37:
Chr6:133851763
GRCh38:
Chr6:133530625
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Conflicting interpretations of pathogenicity
(Jan 13, 2018)
criteria provided, conflicting interpretations
58.
GRCh37:
Chr6:133851713
GRCh38:
Chr6:133530575
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
59.
GRCh37:
Chr6:133789759
GRCh38:
Chr6:133468621
EYA4A233V, A264V, A287VDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Cardiovascular phenotype,
not provided, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J
Uncertain significance
(Oct 15, 2022)
criteria provided, multiple submitters, no conflicts
60.
GRCh37:
Chr6:133844297-133844299
GRCh38:
Chr6:133523159-133523161
EYA4, TARIDY574K, Y526K, Y551K, Y580K, Y520KAutosomal dominant nonsyndromic hearing loss 10Pathogenic
(May 7, 2018)
criteria provided, single submitter
61.
GRCh37:
Chr6:133789798
GRCh38:
Chr6:133468660
EYA4A300D, A246D, A277DCardiovascular phenotype, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J
Conflicting interpretations of pathogenicity
(Aug 17, 2021)
criteria provided, conflicting interpretations
62.
GRCh37:
Chr6:133834033
GRCh38:
Chr6:133512895
EYA4, TARIDT399N, T405N, T430N, T459N, T453NDilated cardiomyopathy 1J, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Jan 11, 2022)
criteria provided, multiple submitters, no conflicts
63.
GRCh37:
Chr6:133767832
GRCh38:
Chr6:133446694
EYA4S50CCardiovascular phenotype, Dilated cardiomyopathy 1J, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Aug 30, 2022)
criteria provided, multiple submitters, no conflicts
64.
GRCh37:
Chr6:133834022
GRCh38:
Chr6:133512884
EYA4, TARIDY449*, Y426*, Y395*, Y401*, Y455*Autosomal dominant nonsyndromic hearing loss 10Likely pathogenic
(Feb 13, 2017)
criteria provided, single submitter
65.
GRCh37:
Chr6:133846312
GRCh38:
Chr6:133525174
TARID, EYA4R587*, R593*, R564*, R539*not provided, Dilated cardiomyopathy 1JPathogenic
(Sep 21, 2022)
criteria provided, multiple submitters, no conflicts
66.
GRCh37:
Chr6:133802715
GRCh38:
Chr6:133481577
EYA4P362L, P339L, P368L, P308L, P314Lnot specified, not provided, Autosomal dominant nonsyndromic hearing loss 10,
Dilated cardiomyopathy 1J, Dilated cardiomyopathy 1J
Uncertain significance
(Jun 9, 2022)
criteria provided, multiple submitters, no conflicts
67.
GRCh37:
Chr6:133785941
GRCh38:
Chr6:133464803
EYA4T250N, T196N, T227NDilated cardiomyopathy 1J, not provided, Cardiovascular phenotype,
Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Conflicting interpretations of pathogenicity
(Oct 14, 2022)
criteria provided, conflicting interpretations
68.
GRCh37:
Chr6:133703584
GRCh38:
Chr6:133382446
EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J
Uncertain significance
(Oct 25, 2022)
criteria provided, multiple submitters, no conflicts
69.
GRCh37:
Chr6:133853210
GRCh38:
Chr6:133532072
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Aug 24, 2021)
criteria provided, multiple submitters, no conflicts
70.
GRCh37:
Chr6:133852957
GRCh38:
Chr6:133531819
TARID, EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Benign/Likely benign
(Jan 13, 2018)
criteria provided, single submitter
71.
GRCh37:
Chr6:133852911
GRCh38:
Chr6:133531773
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Benign/Likely benign
(Jan 13, 2018)
criteria provided, single submitter
72.
GRCh37:
Chr6:133852702
GRCh38:
Chr6:133531564
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 12, 2018)
criteria provided, single submitter
73.
GRCh37:
Chr6:133852693
GRCh38:
Chr6:133531555
TARID, EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
74.
GRCh37:
Chr6:133852603
GRCh38:
Chr6:133531465
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
75.
GRCh37:
Chr6:133852531
GRCh38:
Chr6:133531393
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Conflicting interpretations of pathogenicity
(Jan 13, 2018)
criteria provided, conflicting interpretations
76.
GRCh37:
Chr6:133852454
GRCh38:
Chr6:133531316
TARID, EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J,
Autosomal dominant nonsyndromic hearing loss 10
Uncertain significance
(Aug 20, 2021)
criteria provided, multiple submitters, no conflicts
77.
GRCh37:
Chr6:133852303
GRCh38:
Chr6:133531165
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
78.
GRCh37:
Chr6:133852302
GRCh38:
Chr6:133531164
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Conflicting interpretations of pathogenicity
(Jan 12, 2018)
criteria provided, conflicting interpretations
79.
GRCh37:
Chr6:133852245
GRCh38:
Chr6:133531107
EYA4, TARIDnot provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Benign/Likely benign
(May 15, 2021)
criteria provided, multiple submitters, no conflicts
80.
GRCh37:
Chr6:133852212
GRCh38:
Chr6:133531074
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 12, 2018)
criteria provided, single submitter
81.
GRCh37:
Chr6:133852131
GRCh38:
Chr6:133530993
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Conflicting interpretations of pathogenicity
(Jan 12, 2018)
criteria provided, conflicting interpretations
82.
GRCh37:
Chr6:133852127
GRCh38:
Chr6:133530989
EYA4, TARIDnot provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Benign
(May 11, 2021)
criteria provided, multiple submitters, no conflicts
83.
GRCh37:
Chr6:133852051
GRCh38:
Chr6:133530913
EYA4, TARIDnot provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Benign
(May 11, 2021)
criteria provided, multiple submitters, no conflicts
84.
GRCh37:
Chr6:133851953
GRCh38:
Chr6:133530815
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
85.
GRCh37:
Chr6:133851848
GRCh38:
Chr6:133530710
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Conflicting interpretations of pathogenicity
(Jan 12, 2018)
criteria provided, conflicting interpretations
86.
GRCh37:
Chr6:133851810
GRCh38:
Chr6:133530672
EYA4, TARIDnot provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Benign
(May 11, 2021)
criteria provided, multiple submitters, no conflicts
87.
GRCh37:
Chr6:133851755
GRCh38:
Chr6:133530617
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
88.
GRCh37:
Chr6:133851687
GRCh38:
Chr6:133530549
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
89.
GRCh37:
Chr6:133851601
GRCh38:
Chr6:133530463
EYA4, TARIDnot provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Benign
(May 12, 2021)
criteria provided, multiple submitters, no conflicts
90.
GRCh37:
Chr6:133851456
GRCh38:
Chr6:133530318
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 13, 2018)
criteria provided, single submitter
91.
GRCh37:
Chr6:133851377
GRCh38:
Chr6:133530239
EYA4, TARIDnot provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Benign
(May 11, 2021)
criteria provided, multiple submitters, no conflicts
92.
GRCh37:
Chr6:133851293
GRCh38:
Chr6:133530155
EYA4, TARIDAutosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1JConflicting interpretations of pathogenicity
(Jan 13, 2018)
criteria provided, conflicting interpretations
93.
GRCh37:
Chr6:133851207
GRCh38:
Chr6:133530069
EYA4, TARIDnot provided, Autosomal dominant nonsyndromic hearing loss 10, Dilated cardiomyopathy 1J
Benign
(May 11, 2021)
criteria provided, multiple submitters, no conflicts
94.
GRCh37:
Chr6:133850669
GRCh38:
Chr6:133529531
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Benign
(Jan 13, 2018)
criteria provided, single submitter
95.
GRCh37:
Chr6:133850276
GRCh38:
Chr6:133529138
EYA4, TARIDDilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jan 12, 2018)
criteria provided, single submitter
96.
GRCh37:
Chr6:133849966
GRCh38:
Chr6:133528828
EYA4, TARIDnot provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Benign
(Aug 10, 2021)
criteria provided, multiple submitters, no conflicts
97.
GRCh37:
Chr6:133833915
GRCh38:
Chr6:133512777
EYA4, TARIDnot provided, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Conflicting interpretations of pathogenicity
(Aug 1, 2022)
criteria provided, conflicting interpretations
98.
GRCh37:
Chr6:133802747
GRCh38:
Chr6:133481609
EYA4not specified, Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10
Conflicting interpretations of pathogenicity
(Oct 24, 2022)
criteria provided, conflicting interpretations
99.
GRCh37:
Chr6:133789874
GRCh38:
Chr6:133468736
EYA4Dilated cardiomyopathy 1J, Autosomal dominant nonsyndromic hearing loss 10Uncertain significance
(Jun 20, 2022)
criteria provided, multiple submitters, no conflicts
100.
GRCh37:
Chr6:133789787
GRCh38:
Chr6:133468649
EYA4Cardiovascular phenotype, not provided, Autosomal dominant nonsyndromic hearing loss 10,
Dilated cardiomyopathy 1J
Conflicting interpretations of pathogenicity
(Oct 13, 2022)
criteria provided, conflicting interpretations
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