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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926734copy number variation1nstd209human GRCh38 chr8: 100,706,805-100,706,885 , GRCh37.p13 chr8: 101,719,033-101,719,113 PABPC1
    nsv5910485copy number variation1nstd209human GRCh38 chr8: 100,706,996-100,709,457 , GRCh37.p13 chr8: 101,719,224-101,721,685 PABPC1
    nsv5725513mobile element insertion1nstd211human GRCh38 chr8: 100,702,870-100,702,870 , GRCh37.p13 chr8: 101,715,098-101,715,098 MIR7705, PABPC1
    nsv5716495mobile element insertion1nstd211human GRCh38 chr8: 100,702,824-100,702,824 , GRCh37.p13 chr8: 101,715,052-101,715,052 MIR7705, PABPC1
    nsv5476364copy number variation1nstd206human GRCh38 chr8: 100,719,511-100,720,064 , GRCh37.p13 chr8: 101,731,739-101,732,292 PABPC1
    nsv5474683copy number variation1nstd206human GRCh38 chr8: 100,703,754-100,704,321 , GRCh37.p13 chr8: 101,715,982-101,716,549 PABPC1
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4711919copy number variation2nstd195human GRCh37 chr8: 101,719,225-101,719,226 , GRCh38.p12 chr8: 100,706,997-100,706,998 PABPC1
    nsv4607523copy number variation1nstd183human GRCh37 chr8: 101,730,120-101,732,696 , GRCh38.p12 chr8: 100,717,892-100,720,468 PABPC1
    nsv4606496copy number variation1nstd183human GRCh37 chr8: 101,727,829-101,733,963 , GRCh38.p12 chr8: 100,715,601-100,721,735 , PABPC1
    nsv4496734mobile element insertion1nstd166human GRCh37.p13 chr8: 101,719,323-101,719,323 , GRCh38.p12 chr8: 100,707,095-100,707,095 PABPC1
    nsv4486500mobile element insertion1nstd166human GRCh37.p13 chr8: 101,714,339-101,714,339 , GRCh38.p12 chr8: 100,702,111-100,702,111 MIR7705, PABPC1
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4405077copy number variation1nstd174human GRCh37 chr8: 101,717,259-101,719,030 , GRCh38.p12 chr8: 100,705,031-100,706,802 PABPC1
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv4161801copy number variation1nstd166human GRCh37.p13 chr8: 101,726,691-101,726,950 , GRCh38.p12 chr8: 100,714,463-100,714,722 PABPC1
    nsv3965036insertion1nstd168human GRCh38 chr8: 100,673,434-100,709,584 , GRCh37.p13 chr8: 101,685,662-101,721,812 PABPC1, MIR7705, 1 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
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