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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7096482copy number variation1nstd102humanPathogenic GRCh37 chr4: 100,239,320-100,528,137 , GRCh38.p12 chr4: 99,318,163-99,606,980 ADH1B, ADH1C, 5 more genes
    nsv7054609inversion1nstd229human GRCh38 chr4: 95,257,712-104,152,159 , GRCh37.p13 chr4: 96,178,863-105,073,316 SLC39A8, PABPC1P7, 96 more genes
    nsv7052845inversion1nstd229human GRCh38 chr4: 97,450,222-102,053,198 , GRCh37.p13 chr4: 98,371,373-102,974,355 RNU6-462P, LOC105377345, 58 more genes
    nsv7052661inversion1nstd229human GRCh38 chr4: 96,912,053-103,991,076 , GRCh37.p13 chr4: 97,833,204-104,912,233 MIR1255A, LOC107986297, 86 more genes
    nsv7046928inversion1nstd229human GRCh38 chr4: 95,051,434-103,882,549 , GRCh37.p13 chr4: 95,972,585-104,803,706 PABPC1P7, RN7SL728P, 95 more genes
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv6754886copy number variation1nstd229human GRCh38 chr4: 99,352,537-99,352,572 , GRCh37.p13 chr4: 100,273,694-100,273,729 ADH1C
    nsv6750548copy number variation1nstd229human GRCh38 chr4: 99,332,958-99,343,458 , GRCh37.p13 chr4: 100,254,115-100,264,615 ADH1C
    nsv6749771copy number variation1nstd229human GRCh38 chr4: 99,316,301-99,363,000 , GRCh37.p13 chr4: 100,237,458-100,284,157 ADH1C, ADH1B
    nsv6748951copy number variation1nstd229human GRCh38 chr4: 99,351,745-99,351,885 , GRCh37.p13 chr4: 100,272,902-100,273,042 ADH1C
    nsv6741991copy number variation1nstd229human GRCh38 chr4: 99,312,267-99,367,523 , GRCh37.p13 chr4: 100,233,424-100,288,680 ADH1C, ADH1B
    nsv6630192copy number variation1nstd224human GRCh37 chr4: 99,863,585-100,335,586 , GRCh38.p12 chr4: 98,942,434-99,414,429 ADH1B, ADH5, 15 more genes
    nsv6380028copy number variation1nstd223human GRCh38 chr4: 99,312,267-99,367,523 , GRCh37.p13 chr4: 100,233,424-100,288,680 ADH1B, ADH1C
    nsv6379254copy number variation1nstd223human GRCh38 chr4: 99,335,072-99,335,593 , GRCh37.p13 chr4: 100,256,229-100,256,750 ADH1C
    nsv6376737copy number variation1nstd223human GRCh38 chr4: 99,180,425-99,444,855 , GRCh37.p13 chr4: 100,101,582-100,366,012 ADH7, LOC100507053, 5 more genes
    nsv6311812copy number variation1nstd102humanUncertain significance GRCh37 chr4: 100,239,320-100,544,005 , GRCh38.p12 chr4: 99,318,163-99,622,848 C4orf17, ADH1B, 5 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291428copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060 ADH1A, ADH1B, 157 more genes
    nsv6135624copy number variation1nstd213human GRCh37 chr4: 94,300,000-108,550,001 , GRCh38.p12 chr4: 93,378,849-107,628,845 , ADH1A, 146 more genes
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