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Items: 1 to 20 of 257

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7061563inversion1nstd229human GRCh38 chr8: 27,492,341-29,312,113 , GRCh37.p13 chr8: 27,349,858-29,169,630 LOC100130612, HMBOX1, 37 more genes
    nsv6849231copy number variation1nstd229human GRCh38 chr8: 27,600,061-27,761,033 , GRCh37.p13 chr8: 27,457,578-27,618,550 MIR6843, CCDC25, 6 more genes
    nsv6845919copy number variation1nstd229human GRCh38 chr8: 27,770,325-27,776,131 , GRCh37.p13 chr8: 27,627,842-27,633,648 CCDC25, ESCO2, 1 more genes
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6636640copy number variation1nstd102humanUncertain significance GRCh37 chr8: 27,064,033-28,832,392 , GRCh38.p12 chr8: 27,206,516-28,974,875 ZNF395, PNOC, 39 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6565031inversion1nstd223human GRCh38 chr8: 22,900,235-30,247,902 , GRCh37.p13 chr8: 22,757,748-30,105,418 LOC105379349, MIR6876, 140 more genes
    nsv6424676copy number variation1nstd223human GRCh38 chr8: 27,770,325-27,776,126 , GRCh37.p13 chr8: 27,627,842-27,633,643 ESCO2, CCDC25, 1 more genes
    nsv6423675copy number variation1nstd223human GRCh38 chr8: 27,763,641-27,764,678 , GRCh37.p13 chr8: 27,621,158-27,622,195 CCDC25
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6312637copy number variation2nstd102humanUncertain significance GRCh37 chr8: 27,319,146-28,608,383 , GRCh38.p12 chr8: 27,461,629-28,750,866 EXTL3-AS1, FZD3, 31 more genes
    nsv6301235copy number variation1nstd186human GRCh37 chr8: 27,627,842-27,633,648 , GRCh38.p12 chr8: 27,770,325-27,776,131 CCDC25, ESCO2, 1 more genes
    nsv6137272copy number variation1nstd213human GRCh37 chr8: 26,370,000-35,590,001 , GRCh38.p12 chr8: 26,512,484-35,732,483 ADRA1A, CHRNA2, 141 more genes
    nsv6137044copy number variation1nstd213human GRCh37 chr8: 12,460,000-33,310,001 , GRCh38.p12 chr8: 12,602,491-33,452,483 NAT1, ASAH1, 322 more genes
    nsv6136655copy number variation1nstd213human GRCh37 chr8: 19,630,000-29,910,001 , GRCh38.p12 chr8: 19,772,489-30,052,485 BMP1, BNIP3L, 194 more genes
    nsv6136573copy number variation1nstd213human GRCh37 chr8: 25,790,000-30,640,001 , GRCh38.p12 chr8: 25,932,484-30,782,485 EPHX2, GSR, 99 more genes
    nsv6136029copy number variation1nstd213human GRCh37 chr8: 26,360,000-35,600,001 , GRCh38.p12 chr8: 26,502,484-35,742,483 ADRA1A, CHRNA2, 141 more genes
    nsv6061557insertion1nstd212human GRCh38 chr8: 27,745,159-27,745,159 , GRCh37.p13 chr8: 27,602,676-27,602,676 CCDC25
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