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Items: 1 to 20 of 413

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121296copy number variation1nstd186human GRCh37 chr9: 136,130,254-136,130,422 , GRCh38.p12 chr9|NW_009646201.1: 80,858-81,128 , GRCh38.p12 chr9: 133,254,867-133,255,035 ABO
    nsv5974643inversion1nstd209human GRCh38 chr9: 133,204,664-133,317,417 , GRCh37.p13 chr9: 136,080,051-136,184,252 , GRCh37.p13 chr9|NW_003315925.1: 30,610-143,511 ABO, OBP2B, 2 more genes
    nsv5962360insertion1nstd209human GRCh38 chr9: 133,254,833-133,254,833 , GRCh37.p13 chr9|NW_003315925.1: 80,792-80,792 ABO
    nsv5956714insertion1nstd209human GRCh38 chr9: 133,266,891-133,266,891 , GRCh37.p13 chr9: 136,142,304-136,142,304 , GRCh37.p13 chr9|NW_003315925.1: 92,985-92,985 ABO
    nsv5954275insertion1nstd209human GRCh38 chr9: 133,255,235-133,255,235 , GRCh37.p13 chr9|NW_003315925.1: 81,328-81,328 , GRCh37.p13 chr9: 136,130,622-136,130,622 ABO
    nsv5953421insertion1nstd209human GRCh38 chr9: 133,265,691-133,265,691 , GRCh37.p13 chr9|NW_003315925.1: 91,785-91,785 , GRCh37.p13 chr9: 136,141,102-136,141,102 ABO
    nsv5924166copy number variation1nstd209human GRCh38 chr9: 133,252,413-133,258,229 , GRCh37.p13 chr9: 136,127,800-136,133,620 , GRCh37.p13 chr9|NW_003315925.1: 78,372-84,323 ABO
    nsv5866805copy number variation1nstd209human GRCh38 chr9: 133,261,436-133,265,727 , GRCh37.p13 chr9|NW_003315925.1: 87,530-91,821 , GRCh37.p13 chr9: 136,136,839-136,141,138 ABO
    nsv5865857copy number variation1nstd209human GRCh38 chr9: 133,273,769-133,277,336 , GRCh37.p13 chr9|NW_003315925.1: 99,863-103,430 , GRCh37.p13 chr9: 136,149,185-136,152,788 ABO
    nsv5863061copy number variation1nstd209human GRCh38 chr9: 133,272,169-133,275,405 , GRCh37.p13 chr9|NW_003315925.1: 98,263-101,499 , GRCh37.p13 chr9: 136,147,584-136,150,821 ABO
    nsv5862748copy number variation2nstd209human GRCh38 chr9: 133,251,123-133,258,235 , GRCh37.p13 chr9|NW_003315925.1: 77,080-84,329 , GRCh37.p13 chr9: 136,126,510-136,133,626 ABO
    nsv5862030copy number variation1nstd209human GRCh38 chr9: 133,242,092-133,248,822 , GRCh37.p13 chr9|NW_003315925.1: 68,040-74,779 , GRCh37.p13 chr9: 136,117,479-136,124,209 ABO
    nsv5861225copy number variation1nstd209human GRCh38 chr9: 133,266,528-133,269,927 , GRCh37.p13 chr9: 136,141,942-136,145,339 , GRCh37.p13 chr9|NW_003315925.1: 92,622-96,021 ABO
    nsv5857011copy number variation1nstd209human GRCh38 chr9: 133,269,228-133,277,510 , GRCh37.p13 chr9|NW_003315925.1: 95,322-103,604 , GRCh37.p13 chr9: 136,144,640-136,152,954 ABO
    nsv5855486copy number variation1nstd209human GRCh38 chr9: 133,245,023-133,249,622 , GRCh37.p13 chr9|NW_003315925.1: 70,962-75,579 , GRCh37.p13 chr9: 136,120,410-136,125,009 ABO
    nsv5853156copy number variation1nstd209human GRCh38 chr9: 133,248,323-133,264,677 , GRCh37.p13 chr9|NW_003315925.1: 74,280-90,771 , GRCh37.p13 chr9: 136,123,710-136,140,088 ABO
    nsv5848605copy number variation1nstd209human GRCh38 chr9: 133,266,128-133,276,236 , GRCh37.p13 chr9|NW_003315925.1: 92,222-102,330 , GRCh37.p13 chr9: 136,141,540-136,151,688 ABO
    nsv5847843copy number variation1nstd209human GRCh38 chr9: 133,258,636-133,260,835 , GRCh37.p13 chr9: 136,134,027-136,136,238 , GRCh37.p13 chr9|NW_003315925.1: 84,730-86,929 ABO
    nsv5644406insertion1nstd207human GRCh38 chr9: 133,255,415-133,255,415 , GRCh37.p13 chr9|NW_003315925.1: 81,508-81,508 , GRCh37.p13 chr9: 136,130,802-136,130,802 ABO
    nsv5640658insertion1nstd207human GRCh38 chr9: 133,254,953-133,254,953 , GRCh37.p13 chr9|NW_003315925.1: 81,046-81,046 , GRCh37.p13 chr9: 136,130,340-136,130,340 ABO
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