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Items: 1 to 20 of 322

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147640insertion1nstd232human GRCh37.p13 chr1: 186,287,737-186,287,737 , GRCh38.p12 chr1: 186,318,605-186,318,605 TPR
    nsv7146889insertion1nstd232human GRCh37.p13 chr1: 186,314,828-186,314,828 , GRCh38.p12 chr1: 186,345,696-186,345,696 TPR
    nsv7146460insertion1nstd232human GRCh37.p13 chr1: 186,307,377-186,307,377 , GRCh38.p12 chr1: 186,338,245-186,338,245 TPR
    nsv7146084insertion1nstd232human GRCh37.p13 chr1: 186,296,792-186,296,792 , GRCh38.p12 chr1: 186,327,660-186,327,660 TPR
    nsv7145334insertion1nstd232human GRCh37.p13 chr1: 186,313,710-186,313,710 , GRCh38.p12 chr1: 186,344,578-186,344,578 TPR
    nsv7145168insertion1nstd232human GRCh37.p13 chr1: 186,304,674-186,304,674 , GRCh38.p12 chr1: 186,335,542-186,335,542 TPR
    nsv7144516insertion1nstd232human GRCh37.p13 chr1: 186,310,521-186,310,521 , GRCh38.p12 chr1: 186,341,389-186,341,389 TPR
    nsv7143357copy number variation1nstd232human GRCh37.p13 chr1: 186,310,289-186,310,380 , GRCh38.p12 chr1: 186,341,157-186,341,248 TPR
    nsv7141713insertion1nstd232human GRCh37.p13 chr1: 186,307,378-186,307,378 , GRCh38.p12 chr1: 186,338,246-186,338,246 TPR
    nsv7141115insertion1nstd232human GRCh37.p13 chr1: 186,315,421-186,315,421 , GRCh38.p12 chr1: 186,346,289-186,346,289 TPR
    nsv7138962insertion1nstd232human GRCh37.p13 chr1: 186,305,825-186,305,825 , GRCh38.p12 chr1: 186,336,693-186,336,693 TPR
    nsv7138712copy number variation1nstd232human GRCh37.p13 chr1: 186,330,841-186,330,919 , GRCh38.p12 chr1: 186,361,709-186,361,787 TPR
    nsv7138491copy number variation1nstd232human GRCh37.p13 chr1: 186,324,690-186,324,765 , GRCh38.p12 chr1: 186,355,558-186,355,633 TPR
    nsv7099254copy number variation1nstd231human GRCh38.p12 chr1: 182,376,401-191,898,122 , GRCh37 chr1: 182,345,536-191,867,252 DHX9, GLUL, 99 more genes
    nsv7095494copy number variation1nstd102humanUncertain significance GRCh37 chr1: 185,703,912-186,957,640 , GRCh38.p12 chr1: 185,734,780-186,988,508 RNU6-1240P, PTGS2, 10 more genes
    nsv7053326inversion1nstd229human GRCh38 chr1: 183,856,809-187,909,288 , GRCh37.p13 chr1: 183,825,943-187,878,419 RGL1, TPR, 49 more genes
    nsv6646292copy number variation1nstd229human GRCh38 chr1: 186,355,194-186,355,246 , GRCh37.p13 chr1: 186,324,326-186,324,378 TPR
    nsv6646290copy number variation1nstd229human GRCh38 chr1: 186,305,657-186,311,963 , GRCh37.p13 chr1: 186,274,789-186,281,095 RNU6-1240P, TPR, 1 more genes
    nsv6646217copy number variation1nstd229human GRCh38 chr1: 186,316,161-186,326,718 , GRCh37.p13 chr1: 186,285,293-186,295,850 TPR
    nsv6645859copy number variation1nstd229human GRCh38 chr1: 186,341,600-186,345,469 , GRCh37.p13 chr1: 186,310,732-186,314,601 TPR
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