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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
    nsv7098173copy number variation1nstd102humanUncertain significance GRCh37 chr8: 38,117,538-38,961,219 , GRCh38.p12 chr8: 38,260,020-39,103,700 TM2D2, FGFR1, 14 more genes
    nsv7063861inversion1nstd229human GRCh38 chr8: 38,813,248-38,813,323 , GRCh37.p13 chr8: 38,670,766-38,670,841 TACC1
    nsv6851987copy number variation1nstd229human GRCh38 chr8: 38,765,136-38,769,868 , GRCh37.p13 chr8: 38,622,654-38,627,386 TACC1
    nsv6850729copy number variation1nstd229human GRCh38 chr8: 38,746,435-38,746,546 , GRCh37.p13 chr8: 38,603,953-38,604,064 TACC1
    nsv6848107copy number variation1nstd229human GRCh38 chr8: 38,772,522-38,780,970 , GRCh37.p13 chr8: 38,630,040-38,638,488 TACC1
    nsv6844927copy number variation1nstd229human GRCh38 chr8: 38,814,363-38,958,975 , GRCh37.p13 chr8: 38,671,881-38,816,493 TACC1, PLEKHA2
    nsv6844309copy number variation1nstd229human GRCh38 chr8: 38,748,892-38,766,137 , GRCh37.p13 chr8: 38,606,410-38,623,655 TACC1
    nsv6844178copy number variation1nstd229human GRCh38 chr8: 38,844,145-38,851,789 , GRCh37.p13 chr8: 38,701,663-38,709,307 TACC1
    nsv6842941copy number variation1nstd229human GRCh38 chr8: 38,847,939-38,848,472 , GRCh37.p13 chr8: 38,705,457-38,705,990 TACC1
    nsv6839650copy number variation1nstd229human GRCh38 chr8: 38,572,201-41,442,522 , GRCh37.p13 chr8: 38,429,719-41,300,041 RPL3P10, SNORD65B, 35 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6571060inversion1nstd223human GRCh38 chr8: 38,777,500-38,778,101 , GRCh37.p13 chr8: 38,635,018-38,635,619 TACC1
    nsv6566055inversion1nstd223human GRCh38 chr8: 38,764,231-38,764,923 , GRCh37.p13 chr8: 38,621,749-38,622,441 TACC1
    nsv6558540inversion1nstd223human GRCh38 chr8: 38,755,431-38,756,068 , GRCh37.p13 chr8: 38,612,949-38,613,586 TACC1
    nsv6429678copy number variation1nstd223human GRCh38 chr8: 38,803,797-38,804,542 , GRCh37.p13 chr8: 38,661,315-38,662,060 TACC1
    nsv6426120copy number variation1nstd223human GRCh38 chr8: 38,786,801-38,787,600 , GRCh37.p13 chr8: 38,644,319-38,645,118 TACC1
    nsv6419440copy number variation1nstd223human GRCh38 chr8: 38,786,601-38,787,300 , GRCh37.p13 chr8: 38,644,119-38,644,818 TACC1
    nsv6417035copy number variation1nstd223human GRCh38 chr8: 38,786,501-38,788,600 , GRCh37.p13 chr8: 38,644,019-38,646,118 TACC1
    nsv6416528copy number variation1nstd223human GRCh38 chr8: 38,773,136-38,774,742 , GRCh37.p13 chr8: 38,630,654-38,632,260 TACC1
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