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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5875814copy number variation1nstd209human GRCh38 chr16: 24,924,653-24,926,024 , GRCh37.p13 chr16: 24,935,974-24,937,345 ARHGAP17
    nsv5729690mobile element insertion1nstd211human GRCh38 chr16: 24,936,033-24,936,033 , GRCh37.p13 chr16: 24,947,354-24,947,354 ARHGAP17
    nsv5710876mobile element insertion1nstd211human GRCh38 chr16: 24,951,696-24,951,696 , GRCh37.p13 chr16: 24,963,017-24,963,017 ARHGAP17
    nsv5710078mobile element insertion1nstd211human GRCh38 chr16: 24,922,148-24,922,148 , GRCh37.p13 chr16: 24,933,469-24,933,469 ARHGAP17
    nsv5709452mobile element insertion2nstd211human GRCh38 chr16: 24,982,983-24,982,983 , GRCh37.p13 chr16: 24,994,304-24,994,304 ARHGAP17
    nsv5701961mobile element insertion2nstd211human GRCh38 chr16: 24,991,498-24,991,498 , GRCh37.p13 chr16: 25,002,819-25,002,819 ARHGAP17
    nsv5662936insertion1nstd207human GRCh38 chr16: 24,982,249-24,982,249 , GRCh37.p13 chr16: 24,993,570-24,993,570 ARHGAP17
    nsv5553926mobile element insertion1nstd206human GRCh38 chr16: 24,936,033-24,936,084 , GRCh37.p13 chr16: 24,947,354-24,947,405 ARHGAP17
    nsv5550030insertion1nstd206human GRCh38 chr16: 24,982,268-24,982,292 , GRCh37.p13 chr16: 24,993,589-24,993,613 ARHGAP17
    nsv5522781copy number variation1nstd206human GRCh38 chr16: 24,918,502-24,924,531 , GRCh37.p13 chr16: 24,929,823-24,935,852 , ARHGAP17
    nsv5522680copy number variation1nstd206human GRCh38 chr16: 25,011,477-25,013,447 , GRCh37.p13 chr16: 25,022,798-25,024,768 ARHGAP17
    nsv5521817copy number variation1nstd206human GRCh38 chr16: 24,936,524-24,936,600 , GRCh37.p13 chr16: 24,947,845-24,947,921 ARHGAP17
    nsv5517236copy number variation1nstd206human GRCh38 chr16: 25,003,703-25,004,388 , GRCh37.p13 chr16: 25,015,024-25,015,709 ARHGAP17
    nsv5430213mobile element insertion1nstd206human GRCh38 chr16: 24,991,498-24,991,549 , GRCh37.p13 chr16: 25,002,819-25,002,870 ARHGAP17
    nsv5427372mobile element insertion1nstd206human GRCh38 chr16: 24,922,148-24,922,162 , GRCh37.p13 chr16: 24,933,469-24,933,483 ARHGAP17
    nsv5420484mobile element insertion1nstd206human GRCh38 chr16: 24,951,696-24,951,747 , GRCh37.p13 chr16: 24,963,017-24,963,068 ARHGAP17
    nsv5144563mobile element insertion1nstd203human GRCh38 chr16: 24,991,476-24,991,498 , GRCh37.p13 chr16: 25,002,797-25,002,819 ARHGAP17
    nsv5143395mobile element insertion1nstd203human GRCh38 chr16: 24,982,249-24,982,268 , GRCh37.p13 chr16: 24,993,570-24,993,589 ARHGAP17
    nsv5003262copy number variation1nstd200human GRCh38 chr16: 25,001,816-25,002,824 , GRCh37.p13 chr16: 25,013,137-25,014,145 ARHGAP17
    nsv5003261copy number variation1nstd200human GRCh38 chr16: 24,983,847-24,984,107 , GRCh37.p13 chr16: 24,995,168-24,995,428 ARHGAP17
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