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Items: 1 to 20 of 439

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131644insertion1nstd186human GRCh37 chr15: 100,343,324-100,343,375 , GRCh38.p12 chr15: 99,803,119-99,803,170 DNM1P46
    nsv6131324insertion1nstd186human GRCh37 chr15: 100,331,081-100,331,092 , GRCh38.p12 chr15: 99,790,876-99,790,887 DNM1P46, RN7SL484P
    nsv6121161copy number variation1nstd186human GRCh37 chr15: 100,340,009-100,340,393 , GRCh38.p12 chr15: 99,799,804-99,800,188 DNM1P46
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv5976309insertion1nstd209human GRCh38 chr15: 99,799,856-99,799,856 , GRCh37.p13 chr15: 100,340,061-100,340,061 DNM1P46
    nsv5973246inversion1nstd209human GRCh38 chr15: 97,535,582-101,746,493 , GRCh37.p13 chr15: 98,078,812-102,286,696 , ALDH1A3, 71 more genes
    nsv5969339insertion1nstd209human GRCh38 chr15: 99,803,120-99,803,120 , GRCh37.p13 chr15: 100,343,325-100,343,325 DNM1P46
    nsv5942541copy number variation1nstd209human GRCh38 chr15: 99,798,371-99,798,469 , GRCh37.p13 chr15: 100,338,576-100,338,674 DNM1P46
    nsv5874881copy number variation1nstd209human GRCh38 chr15: 99,800,507-99,804,071 , GRCh37.p13 chr15: 100,340,712-100,344,276 DNM1P46
    nsv5869995copy number variation1nstd209human GRCh38 chr15: 99,800,506-99,803,218 , GRCh37.p13 chr15: 100,340,711-100,343,423 DNM1P46
    nsv5709366mobile element insertion2nstd211human GRCh38 chr15: 99,803,119-99,803,119 , GRCh37.p13 chr15: 100,343,324-100,343,324 DNM1P46
    nsv5672734copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 99,192,811-101,791,668 , GRCh38.p12 chr15: 98,649,582-101,251,463 ALDH1A3, IGF1R, 43 more genes
    nsv5663840insertion1nstd207human GRCh38 chr15: 99,799,779-99,799,779 , GRCh37.p13 chr15: 100,339,984-100,339,984 DNM1P46
    nsv5663605insertion1nstd207human GRCh38 chr15: 99,800,084-99,800,084 , GRCh37.p13 chr15: 100,340,289-100,340,289 DNM1P46
    nsv5663338insertion1nstd207human GRCh38 chr15: 99,795,452-99,795,452 , GRCh37.p13 chr15: 100,335,657-100,335,657 DNM1P46
    nsv5662428insertion1nstd207human GRCh38 chr15: 99,790,836-99,790,836 , GRCh37.p13 chr15: 100,331,041-100,331,041 DNM1P46, RN7SL484P
    nsv5658013insertion1nstd207human GRCh38 chr15: 99,792,841-99,792,841 , GRCh37.p13 chr15: 100,333,046-100,333,046 DNM1P46
    nsv5655093insertion1nstd207human GRCh38 chr15: 99,799,739-99,799,739 , GRCh37.p13 chr15: 100,339,944-100,339,944 DNM1P46
    nsv5652213insertion1nstd207human GRCh38 chr15: 99,799,974-99,799,974 , GRCh37.p13 chr15: 100,340,179-100,340,179 DNM1P46
    nsv5649479insertion1nstd207human GRCh38 chr15: 99,798,388-99,798,388 , GRCh37.p13 chr15: 100,338,593-100,338,593 DNM1P46
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