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Items: 1 to 20 of 2441

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122030copy number variation1nstd186human GRCh37 chr11: 131,468,696-131,468,789 , GRCh38.p12 chr11: 131,598,802-131,598,895 NTM
    nsv6114060copy number variation1nstd186human GRCh37 chr11: 131,938,957-131,939,999 , GRCh38.p12 chr11: 132,069,063-132,070,105 NTM
    nsv6113323mobile element insertion1nstd186human GRCh37 chr11: 131,324,637-131,324,637 , GRCh38.p12 chr11: 131,454,743-131,454,743 NTM
    nsv5978895insertion1nstd209human GRCh38 chr11: 131,424,600-131,424,600 , GRCh37.p13 chr11: 131,294,494-131,294,494 NTM
    nsv5977905insertion1nstd209human GRCh38 chr11: 131,491,426-131,491,426 , GRCh37.p13 chr11: 131,361,320-131,361,320 NTM
    nsv5974928insertion1nstd209human GRCh38 chr11: 131,789,429-131,789,429 , GRCh37.p13 chr11: 131,659,323-131,659,323 NTM
    nsv5973458insertion1nstd209human GRCh38 chr11: 131,598,732-131,598,732 , GRCh37.p13 chr11: 131,468,626-131,468,626 NTM
    nsv5972430insertion1nstd209human GRCh38 chr11: 132,282,976-132,282,976 , GRCh37.p13 chr11: 132,152,870-132,152,870 NTM, NTM-IT
    nsv5971713insertion1nstd209human GRCh38 chr11: 131,730,721-131,730,721 , GRCh37.p13 chr11: 131,600,615-131,600,615 NTM
    nsv5969805insertion1nstd209human GRCh38 chr11: 131,763,700-131,763,700 , GRCh37.p13 chr11: 131,633,594-131,633,594 NTM
    nsv5969711insertion1nstd209human GRCh38 chr11: 131,493,392-131,493,392 , GRCh37.p13 chr11: 131,363,286-131,363,286 NTM
    nsv5969602insertion1nstd209human GRCh38 chr11: 131,454,729-131,454,729 , GRCh37.p13 chr11: 131,324,623-131,324,623 NTM
    nsv5969400insertion1nstd209human GRCh38 chr11: 131,521,344-131,521,344 , GRCh37.p13 chr11: 131,391,238-131,391,238 NTM
    nsv5969278insertion1nstd209human GRCh38 chr11: 132,125,729-132,125,729 , GRCh37.p13 chr11: 131,995,623-131,995,623 NTM
    nsv5968728insertion1nstd209human GRCh38 chr11: 131,878,595-131,878,595 , GRCh37.p13 chr11: 131,748,489-131,748,489 LOC107984413, NTM
    nsv5926456copy number variation1nstd209human GRCh38 chr11: 132,239,979-132,240,029 , GRCh37.p13 chr11: 132,109,873-132,109,923 NTM
    nsv5924193copy number variation1nstd209human GRCh38 chr11: 131,978,533-131,978,595 , GRCh37.p13 chr11: 131,848,427-131,848,489 NTM
    nsv5924079copy number variation1nstd209human GRCh38 chr11: 132,070,112-132,070,423 , GRCh37.p13 chr11: 131,940,006-131,940,317 NTM
    nsv5922915copy number variation1nstd209human GRCh38 chr11: 132,054,373-132,060,409 , GRCh37.p13 chr11: 131,924,267-131,930,303 NTM
    nsv5922242copy number variation1nstd209human GRCh38 chr11: 131,956,728-131,956,927 , GRCh37.p13 chr11: 131,826,622-131,826,821 NTM
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