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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919018copy number variation1nstd209human GRCh38 chr11: 75,846,379-75,846,596 , GRCh37.p13 chr11: 75,557,424-75,557,641 UVRAG
    nsv5907731copy number variation1nstd209human GRCh38 chr11: 75,924,416-75,924,465 , GRCh37.p13 chr11: 75,635,460-75,635,509 UVRAG
    nsv5728267mobile element insertion2nstd211human GRCh38 chr11: 75,819,021-75,819,021 , GRCh37.p13 chr11: 75,530,066-75,530,066 UVRAG
    nsv5723573mobile element insertion1nstd211human GRCh38 chr11: 76,117,392-76,117,392 , GRCh37.p13 chr11: 75,828,436-75,828,436 UVRAG
    nsv5722394mobile element insertion2nstd211human GRCh38 chr11: 76,132,636-76,132,636 , GRCh37.p13 chr11: 75,843,680-75,843,680 UVRAG
    nsv5712741mobile element insertion1nstd211human GRCh38 chr11: 75,884,411-75,884,411 , GRCh37.p13 chr11: 75,595,455-75,595,455 UVRAG
    nsv5703964mobile element insertion1nstd211human GRCh38 chr11: 76,092,517-76,092,517 , GRCh37.p13 chr11: 75,803,561-75,803,561 UVRAG
    nsv5702185mobile element insertion1nstd211human GRCh38 chr11: 76,050,658-76,050,658 , GRCh37.p13 chr11: 75,761,702-75,761,702 UVRAG
    nsv5701857mobile element insertion1nstd211human GRCh38 chr11: 75,900,152-75,900,152 , GRCh37.p13 chr11: 75,611,196-75,611,196 UVRAG
    nsv5701392mobile element insertion1nstd211human GRCh38 chr11: 76,091,394-76,091,394 , GRCh37.p13 chr11: 75,802,438-75,802,438 UVRAG
    nsv5694561mobile element insertion1nstd211human GRCh38 chr11: 75,941,362-75,941,362 , GRCh37.p13 chr11: 75,652,406-75,652,406 UVRAG
    nsv5651077insertion1nstd207human GRCh38 chr11: 75,877,562-75,877,562 , GRCh37.p13 chr11: 75,588,606-75,588,606 UVRAG
    nsv5590091copy number variation1nstd207human GRCh38 chr11: 75,878,262-75,878,341 , GRCh37.p13 chr11: 75,589,306-75,589,385 UVRAG
    nsv5558582mobile element insertion1nstd206human GRCh38 chr11: 75,819,021-75,819,072 , GRCh37.p13 chr11: 75,530,066-75,530,117 UVRAG
    nsv5554668mobile element insertion1nstd206human GRCh38 chr11: 76,132,636-76,132,687 , GRCh37.p13 chr11: 75,843,680-75,843,731 UVRAG
    nsv5512238copy number variation1nstd206human GRCh38 chr11: 75,929,025-75,929,099 , GRCh37.p13 chr11: 75,640,069-75,640,143 UVRAG
    nsv5501931copy number variation1nstd206human GRCh38 chr11: 75,847,064-76,036,774 , GRCh37.p13 chr11: 75,558,109-75,747,818 UVRAG, PPP1R1AP1, 1 more genes
    nsv5501665copy number variation1nstd206human GRCh38 chr11: 75,955,663-75,955,812 , GRCh37.p13 chr11: 75,666,707-75,666,856 UVRAG
    nsv5497721copy number variation1nstd206human GRCh38 chr11: 75,842,840-75,843,841 , GRCh37.p13 chr11: 75,553,885-75,554,886 UVRAG
    nsv5494860copy number variation1nstd206human GRCh38 chr11: 75,846,379-75,846,597 , GRCh37.p13 chr11: 75,557,424-75,557,642 UVRAG
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