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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7097903copy number variation1nstd102humanUncertain significance GRCh37 chr8: 41,518,984-42,698,237 , GRCh38.p12 chr8: 41,661,466-42,843,094 DKK4, KAT6A, 22 more genes
    nsv7097662copy number variation2nstd102humanUncertain significance GRCh37 chr8: 41,518,984-43,054,712 , GRCh38.p12 chr8: 41,661,466-43,199,569 LOC101059972, IKBKB-DT, 31 more genes
    nsv7073030inversion1nstd229human GRCh38 chr8: 42,166,848-42,166,884 , GRCh37.p13 chr8: 42,024,366-42,024,402 AP3M2
    nsv7065639inversion1nstd229human GRCh38 chr8: 40,079,981-42,715,940 , GRCh37.p13 chr8: 39,937,500-42,571,083 LOC105379390, RPL17P30, 44 more genes
    nsv6852219copy number variation1nstd229human GRCh38 chr8: 42,171,192-42,213,015 , GRCh37.p13 chr8: 42,028,710-42,070,533 PLAT, AP3M2
    nsv6851328copy number variation1nstd229human GRCh38 chr8: 42,165,429-42,168,718 , GRCh37.p13 chr8: 42,022,947-42,026,236 AP3M2
    nsv6842138copy number variation1nstd229human GRCh38 chr8: 42,165,769-42,165,951 , GRCh37.p13 chr8: 42,023,287-42,023,469 AP3M2
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6431311copy number variation1nstd223human GRCh38 chr8: 42,138,981-42,172,661 , GRCh37.p13 chr8: 41,996,499-42,030,179 AP3M2, LOC107986939
    nsv6421709copy number variation1nstd223human GRCh38 chr8: 42,165,428-42,168,716 , GRCh37.p13 chr8: 42,022,946-42,026,234 AP3M2
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6136047copy number variation1nstd213human GRCh37 chr8: 41,160,000-42,320,001 , GRCh38.p12 chr8: 41,302,481-42,462,483 SLC20A2, GOLGA7, 27 more genes
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5695198mobile element insertion1nstd211human GRCh38 chr8: 42,163,318-42,163,318 , GRCh37.p13 chr8: 42,020,836-42,020,836 AP3M2
    nsv5564499copy number variation1nstd102humanUncertain significance GRCh37 chr8: 41,905,876-42,188,497 , GRCh38.p12 chr8: 42,048,358-42,330,979 LOC101059972, IKBKB-DT, 8 more genes
    nsv5398758mobile element insertion1nstd206human GRCh38 chr8: 42,163,318-42,163,369 , GRCh37.p13 chr8: 42,020,836-42,020,887 AP3M2
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
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