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Items: 1 to 20 of 539

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112736copy number variation1nstd102humanPathogenic GRCh37 chr10: 48,301,535-51,807,296 , GRCh38.p12 chr10: 45,999,930-49,959,916 SHLD2P3, LOC100420617, 95 more genes
    nsv5971751inversion1nstd209human GRCh38 chr10: 48,640,771-48,658,698 , GRCh37.p13 chr10: 49,848,816-49,866,743 ARHGAP22
    nsv5959941insertion1nstd209human GRCh38 chr10: 48,655,068-48,655,068 , GRCh37.p13 chr10: 49,863,113-49,863,113 ARHGAP22
    nsv5957862insertion1nstd209human GRCh38 chr10: 48,651,667-48,651,667 , GRCh37.p13 chr10: 49,859,712-49,859,712 ARHGAP22
    nsv5950753insertion1nstd209human GRCh38 chr10: 48,577,797-48,577,797 , GRCh37.p13 chr10: 49,785,842-49,785,842 ARHGAP22
    nsv5917339copy number variation1nstd209human GRCh38 chr10: 48,483,855-48,484,081 , GRCh37.p13 chr10: 49,691,898-49,692,124 ARHGAP22
    nsv5916113copy number variation1nstd209human GRCh38 chr10: 45,791,488-50,132,032 , GRCh37.p13 chr10|NW_003871068.1: 62,603-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,891,792 , LINC02675, 111 more genes
    nsv5914502copy number variation1nstd209human GRCh38 chr10: 45,768,833-50,109,449 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 39,948-2,281,126 , AGAP13P, 111 more genes
    nsv5728466mobile element insertion1nstd211human GRCh38 chr10: 48,510,449-48,510,449 , GRCh37.p13 chr10: 49,718,492-49,718,492 ARHGAP22, ARHGAP22-IT1
    nsv5726897mobile element insertion1nstd211human GRCh38 chr10: 48,510,464-48,510,464 , GRCh37.p13 chr10: 49,718,507-49,718,507 ARHGAP22-IT1, ARHGAP22
    nsv5711666mobile element insertion1nstd211human GRCh38 chr10: 48,487,114-48,487,114 , GRCh37.p13 chr10: 49,695,157-49,695,157 ARHGAP22
    nsv5708617mobile element insertion1nstd211human GRCh38 chr10: 48,502,087-48,502,087 , GRCh37.p13 chr10: 49,710,130-49,710,130 ARHGAP22
    nsv5699645mobile element insertion1nstd211human GRCh38 chr10: 48,483,727-48,483,727 , GRCh37.p13 chr10: 49,691,770-49,691,770 ARHGAP22
    nsv5636897insertion2nstd207human GRCh38 chr10: 48,655,068-48,655,068 , GRCh37.p13 chr10: 49,863,113-49,863,113 ARHGAP22
    nsv5555531mobile element insertion1nstd206human GRCh38 chr10: 48,510,464-48,510,515 , GRCh37.p13 chr10: 49,718,507-49,718,558 ARHGAP22-IT1, ARHGAP22
    nsv5536155insertion1nstd206human GRCh38 chr10: 48,474,643-48,474,654 , GRCh37.p13 chr10: 49,682,686-49,682,697 ARHGAP22
    nsv5534030insertion1nstd206human GRCh38 chr10: 48,429,738-48,429,781 , GRCh37.p13 chr10: 49,637,781-49,637,824 ARHGAP22, MAPK8
    nsv5493857copy number variation1nstd206human GRCh38 chr10: 48,485,245-48,485,300 , GRCh37.p13 chr10: 49,693,288-49,693,343 ARHGAP22
    nsv5491547copy number variation1nstd206human GRCh38 chr10: 48,648,489-48,648,601 , GRCh37.p13 chr10: 49,856,534-49,856,646 ARHGAP22
    nsv5489495copy number variation1nstd206human GRCh38 chr10: 48,550,203-48,550,302 , GRCh37.p13 chr10: 49,758,248-49,758,347 ARHGAP22
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