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Items: 1 to 20 of 245

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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
    nsv6422490copy number variation1nstd223human GRCh38 chr8: 22,016,438-22,022,912 , GRCh37.p13 chr8: 21,873,949-21,880,423 NPM2
    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
    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
    nsv6067126insertion1nstd212human GRCh38 chr8: 22,021,592-22,021,592 , GRCh37.p13 chr8: 21,879,103-21,879,103 NPM2
    nsv5954342insertion1nstd209human GRCh38 chr8: 22,021,592-22,021,592 , GRCh37.p13 chr8: 21,879,103-21,879,103 NPM2
    nsv5722721mobile element insertion2nstd211human GRCh38 chr8: 22,021,611-22,021,611 , GRCh37.p13 chr8: 21,879,122-21,879,122 NPM2
    nsv5631952insertion1nstd207human GRCh38 chr8: 22,021,592-22,021,592 , GRCh37.p13 chr8: 21,879,103-21,879,103 NPM2
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