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Items: 1 to 20 of 662

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127404copy number variation1nstd186human GRCh37 chr19: 41,338,779-41,370,779 , GRCh38.p12 chr19: 40,832,874-40,864,874 CYP2A6
    nsv6124659copy number variation1nstd186human GRCh37 chr19: 41,352,226-41,384,122 , GRCh38.p12 chr19: 40,846,321-40,878,217 CYP2A6, CYP2A7
    nsv6123408copy number variation1nstd186human GRCh37 chr19: 41,355,847-41,387,566 , GRCh38.p12 chr19: 40,849,942-40,881,661 CYP2A6, CYP2A7
    nsv5980242insertion1nstd209human GRCh38 chr19: 40,848,973-40,848,973 , GRCh37.p13 chr19: 41,354,878-41,354,878 CYP2A6
    nsv5977639inversion1nstd209human GRCh38 chr19: 40,827,499-41,120,720 , GRCh37.p13 chr19: 41,333,404-41,626,625 , CYP2A6, 8 more genes
    nsv5940366copy number variation1nstd209human GRCh38 chr19: 40,849,894-40,881,681 , GRCh37.p13 chr19: 41,355,799-41,387,586 CYP2A6, CYP2A7
    nsv5938187copy number variation1nstd209human GRCh38 chr19: 40,843,635-40,875,393 , GRCh37.p13 chr19: 41,349,540-41,381,298 CYP2A7, CYP2A6
    nsv5935083copy number variation1nstd209human GRCh38 chr19: 40,838,774-40,869,289 , GRCh37.p13 chr19: 41,344,679-41,375,194 CYP2A6
    nsv5881816copy number variation2nstd209human GRCh38 chr19: 40,844,224-40,850,428 , GRCh37.p13 chr19: 41,350,129-41,356,333 CYP2A6
    nsv5879934copy number variation2nstd209human GRCh38 chr19: 40,836,760-40,843,602 , GRCh37.p13 chr19: 41,342,665-41,349,507 CYP2A6
    nsv5877452copy number variation2nstd209human GRCh38 chr19: 40,849,758-40,864,941 , GRCh37.p13 chr19: 41,355,663-41,370,846 CYP2A6
    nsv5874528copy number variation2nstd209human GRCh38 chr19: 40,839,532-40,842,493 , GRCh37.p13 chr19: 41,345,437-41,348,398 CYP2A6
    nsv5869880copy number variation2nstd209human GRCh38 chr19: 40,837,485-40,843,653 , GRCh37.p13 chr19: 41,343,390-41,349,558 CYP2A6
    nsv5664156insertion1nstd207human GRCh38 chr19: 40,846,598-40,846,598 , GRCh37.p13 chr19: 41,352,503-41,352,503 CYP2A6
    nsv5592987copy number variation1nstd207human GRCh38 chr19: 40,848,929-40,849,028 , GRCh37.p13 chr19: 41,354,834-41,354,933 CYP2A6
    nsv5587994copy number variation1nstd207human GRCh38 chr19: 40,833,931-40,864,823 , GRCh37.p13 chr19: 41,339,836-41,370,728 CYP2A6
    nsv5564058sequence alteration1nstd206human GRCh38 chr19: 40,827,060-41,121,102 , GRCh37.p13 chr19: 41,332,965-41,627,007 , CYP2F2P, 9 more genes
    nsv5526425copy number variation1nstd206human GRCh38 chr19: 40,832,874-40,843,468 , GRCh37.p13 chr19: 41,338,779-41,349,373 CYP2A6
    nsv5525401copy number variation1nstd206human GRCh38 chr19: 40,838,833-40,869,698 , GRCh37.p13 chr19: 41,344,738-41,375,603 CYP2A6
    nsv5520883copy number variation1nstd206human GRCh38 chr19: 40,846,321-40,878,217 , GRCh37.p13 chr19: 41,352,226-41,384,122 CYP2A7, CYP2A6
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