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Items: 1 to 20 of 208

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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
    nsv7098901copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 21,925,038-26,372,195 , GRCh38.p12 chr8: 22,067,527-26,514,679 BMP1, POLR3D, 95 more genes
    nsv7073429inversion1nstd229human GRCh38 chr8: 22,689,880-24,095,801 , GRCh37.p13 chr8: 22,547,393-23,953,314 TNFRSF10B, RNU1-148P, 34 more genes
    nsv6841448copy number variation1nstd229human GRCh38 chr8: 23,854,719-23,854,756 , GRCh37.p13 chr8: 23,712,232-23,712,269 STC1
    nsv6841173copy number variation1nstd229human GRCh38 chr8: 23,851,171-23,851,335 , GRCh37.p13 chr8: 23,708,684-23,708,848 STC1
    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
    nsv6429716copy number variation1nstd223human GRCh38 chr8: 22,969,514-24,288,515 , GRCh37.p13 chr8: 22,827,027-24,146,028 NKX3-1, LOC107984124, 27 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
    nsv6137266copy number variation1nstd213human GRCh37 chr8: 22,950,000-24,240,001 , GRCh38.p12 chr8: 23,092,487-24,382,488 TNFRSF10D, CHMP7, 25 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
    nsv6136570copy number variation1nstd213human GRCh37 chr8: 22,760,000-24,790,001 , GRCh38.p12 chr8: 22,902,487-24,932,488 LOXL2, NEFM, 38 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
    nsv5919722copy number variation1nstd209human GRCh38 chr8: 23,851,535-23,851,594 , GRCh37.p13 chr8: 23,709,048-23,709,107 STC1
    nsv5379155translocation1nstd200human GRCh38 chr8: 23,845,090-23,845,090 , GRCh38 chr8: 23,845,172-23,845,172 , GRCh37.p13 chr8: 23,702,685-23,702,685 , GRCh37.p13 chr8: 23,702,603-23,702,603 STC1
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