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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    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
    nsv6842532copy number variation1nstd229human GRCh38 chr8: 21,982,501-22,396,600 , GRCh37.p13 chr8: 21,840,012-22,254,113 SFTPC, BMP1, 16 more genes
    nsv6842345copy number variation1nstd229human GRCh38 chr8: 21,739,201-22,308,765 , GRCh37.p13 chr8: 21,596,713-22,166,278 FHIP2B, FGF17, 17 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    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
    nsv6315176copy number variation1nstd102humanPathogenic GRCh37 chr8: 19,779,604-26,531,980 , GRCh38.p12 chr8: 19,922,093-26,674,463 TNFRSF10C, TNFRSF10A, 121 more genes
    nsv6313650copy number variation1nstd102humanUncertain significance GRCh37 chr8: 21,303,187-22,230,498 , GRCh38.p12 chr8: 21,445,676-22,372,985 OR6R2P, FGF17, 19 more genes
    nsv6312718copy number variation2nstd102humanUncertain significance GRCh37 chr8: 21,900,440-23,564,111 , GRCh38.p12 chr8: 22,042,929-23,706,598 LOC105379327, RPL23AP55, 56 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
    nsv6136658copy number variation1nstd213human GRCh37 chr8: 21,490,000-22,700,001 , GRCh38.p12 chr8: 21,632,489-22,842,488 POLR3D, PHYHIP, 37 more genes
    nsv6136657copy number variation1nstd213human GRCh37 chr8: 20,690,000-22,620,001 , GRCh38.p12 chr8: 20,832,489-22,762,488 BMP1, POLR3D, 42 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
    nsv6136312copy number variation1nstd213human GRCh37 chr8: 12,460,000-25,900,001 , GRCh38.p12 chr8: 12,602,491-26,042,485 NAT1, NAT2, 195 more genes
    nsv6136241copy number variation1nstd213human GRCh37 chr8: 12,490,000-25,900,001 , GRCh38.p12 chr8: 12,632,491-26,042,485 NAT1, NAT2, 194 more genes
    nsv5492539copy number variation1nstd206human GRCh38 chr8: 22,048,886-22,048,972 , GRCh37.p13 chr8: 21,906,397-21,906,483 DMTN, FGF17
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4457278copy number variation1nstd102humanUncertain significance GRCh37 chr8: 21,840,451-22,037,635 , GRCh38.p12 chr8: 21,982,940-22,180,122 FGF17, FHIP2B, 9 more genes
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