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Items: 1 to 20 of 684

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129812mobile element insertion1nstd186human GRCh37 chr22: 18,136,636-18,136,687 , GRCh38.p12 chr22: 17,653,870-17,653,921 BCL2L13
    nsv6126546copy number variation1nstd186human GRCh37 chr22: 18,126,571-18,129,555 , GRCh38.p12 chr22: 17,643,805-17,646,789 BCL2L13
    nsv6124463copy number variation1nstd186human GRCh37 chr22: 18,141,467-18,144,628 , GRCh38.p12 chr22: 17,658,701-17,661,862 BCL2L13
    nsv5978148insertion1nstd209human GRCh38 chr22: 17,644,644-17,644,644 , GRCh37.p13 chr22: 18,127,410-18,127,410 BCL2L13
    nsv5978025insertion1nstd209human GRCh38 chr22: 17,717,357-17,717,357 , GRCh37.p13 chr22: 18,200,123-18,200,123 BCL2L13
    nsv5976399inversion1nstd209human GRCh38 chr22: 17,577,704-20,098,016 , GRCh37.p13 chr22: 18,057,770-20,703,815 , ARVCF, 90 more genes
    nsv5969613insertion1nstd209human GRCh38 chr22: 17,653,856-17,653,856 , GRCh37.p13 chr22: 18,136,622-18,136,622 BCL2L13
    nsv5966330copy number variation1nstd209human GRCh38 chr22: 17,658,930-17,661,861 , GRCh37.p13 chr22: 18,141,696-18,144,627 BCL2L13
    nsv5965337copy number variation1nstd209human GRCh38 chr22: 17,636,020-17,646,732 , GRCh37.p13 chr22: 18,118,786-18,129,498 BCL2L13
    nsv5964251copy number variation1nstd209human GRCh38 chr22: 17,644,479-17,648,243 , GRCh37.p13 chr22: 18,127,245-18,131,009 BCL2L13
    nsv5959090copy number variation1nstd209human GRCh38 chr22: 17,679,935-17,680,232 , GRCh37.p13 chr22: 18,162,701-18,162,998 BCL2L13
    nsv5958825copy number variation1nstd209human GRCh38 chr22: 17,667,406-17,667,743 , GRCh37.p13 chr22: 18,150,172-18,150,509 BCL2L13
    nsv5952804copy number variation1nstd209human GRCh38 chr22: 17,626,574-17,627,196 , GRCh37.p13 chr22: 18,109,340-18,109,962 BCL2L13, ATP6V1E1
    nsv5951460copy number variation1nstd209human GRCh38 chr22: 17,643,774-17,647,133 , GRCh37.p13 chr22: 18,126,540-18,129,899 BCL2L13
    nsv5949724copy number variation1nstd209human GRCh38 chr22: 17,643,912-17,646,732 , GRCh37.p13 chr22: 18,126,678-18,129,498 BCL2L13
    nsv5948516copy number variation1nstd209human GRCh38 chr22: 17,654,145-17,654,461 , GRCh37.p13 chr22: 18,136,911-18,137,227 BCL2L13
    nsv5886799copy number variation1nstd209human GRCh38 chr22: 17,709,018-17,710,617 , GRCh37.p13 chr22: 18,191,784-18,193,383 BCL2L13
    nsv5883522copy number variation1nstd209human GRCh38 chr22: 17,643,858-17,646,457 , GRCh37.p13 chr22: 18,126,624-18,129,223 BCL2L13
    nsv5881488copy number variation1nstd209human GRCh38 chr22: 17,659,180-17,661,829 , GRCh37.p13 chr22: 18,141,946-18,144,595 BCL2L13
    nsv5726939mobile element insertion1nstd211human GRCh38 chr22: 17,672,828-17,672,828 , GRCh37.p13 chr22: 18,155,594-18,155,594 BCL2L13
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