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Items: 1 to 20 of 346

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139697copy number variation1nstd232human GRCh37.p13 chr8: 87,157,409-87,157,511 , GRCh38.p12 chr8: 86,145,180-86,145,282 ATP6V0D2
    nsv7098039copy number variation1nstd102humanUncertain significance GRCh37 chr8: 86,053,597-87,755,855 , GRCh38.p12 chr8: 85,141,362-86,743,627 UBE2Q2P10, LOC107986954, 40 more genes
    nsv7076485inversion1nstd229human GRCh38 chr8: 86,146,151-86,146,198 , GRCh37.p13 chr8: 87,158,380-87,158,427 ATP6V0D2
    nsv7075262inversion1nstd229human GRCh38 chr8: 83,096,825-86,720,422 , GRCh37.p13 chr8: 84,009,060-87,732,650 REXO1L1P, LOC100422614, 54 more genes
    nsv7066667inversion1nstd229human GRCh38 chr8: 86,085,307-86,165,263 , GRCh37.p13 chr8: 87,097,536-87,177,492 ATP6V0D2
    nsv7066492inversion1nstd229human GRCh38 chr8: 86,121,003-86,124,924 , GRCh37.p13 chr8: 87,133,232-87,137,153 ATP6V0D2
    nsv6854981copy number variation1nstd229human GRCh38 chr8: 86,127,468-86,138,628 , GRCh37.p13 chr8: 87,139,697-87,150,857 ATP6V0D2
    nsv6852197copy number variation1nstd229human GRCh38 chr8: 86,104,594-86,109,795 , GRCh37.p13 chr8: 87,116,823-87,122,024 ATP6V0D2
    nsv6848909copy number variation1nstd229human GRCh38 chr8: 85,503,608-86,382,764 , GRCh37.p13 chr8: 86,415,837-87,394,993 REXO1L1P, WWP1-AS1, 22 more genes
    nsv6848637copy number variation1nstd229human GRCh38 chr8: 86,097,883-86,163,636 , GRCh37.p13 chr8: 87,110,112-87,175,865 ATP6V0D2
    nsv6847401copy number variation1nstd229human GRCh38 chr8: 86,118,353-86,118,723 , GRCh37.p13 chr8: 87,130,582-87,130,952 ATP6V0D2
    nsv6847092copy number variation1nstd229human GRCh38 chr8: 86,150,477-86,150,516 , GRCh37.p13 chr8: 87,162,706-87,162,745 ATP6V0D2
    nsv6845831copy number variation1nstd229human GRCh38 chr8: 86,122,005-86,122,931 , GRCh37.p13 chr8: 87,134,234-87,135,160 ATP6V0D2
    nsv6844413copy number variation1nstd229human GRCh38 chr8: 86,047,213-86,312,908 , GRCh37.p13 chr8: 87,059,442-87,325,137 SLC7A13, PSKH2, 2 more genes
    nsv6841116copy number variation1nstd229human GRCh38 chr8: 86,115,379-86,125,976 , GRCh37.p13 chr8: 87,127,608-87,138,205 ATP6V0D2
    nsv6841026copy number variation1nstd229human GRCh38 chr8: 86,139,932-86,148,733 , GRCh37.p13 chr8: 87,152,161-87,160,962 ATP6V0D2
    nsv6637803copy number variation1nstd102humanUncertain significance GRCh37 chr8: 87,010,235-91,879,538 , GRCh38.p12 chr8: 85,998,006-90,867,310 LOC105375633, NTAN1P2, 49 more genes
    nsv6637601copy number variation1nstd102humanUncertain significance GRCh37 chr8: 86,841,155-88,126,932 , GRCh38.p12 chr8: 85,828,926-87,114,704 WWP1-AS1, MIOXP1, 18 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6635128copy number variation1nstd227human GRCh38.p12 chr8: 86,154,167-86,318,484 , GRCh37 chr8: 87,166,396-87,330,713 SLC7A13, ATP6V0D2, 1 more genes
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