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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5671625inversion1nstd207human GRCh38 chr8: 7,301,025-12,600,730 , GRCh37.p13 chr8: 7,158,547-12,458,239 , BLK, 188 more genes
    nsv5483576copy number variation1nstd206human GRCh38 chr8: 11,320,693-11,320,822 , GRCh37.p13 chr8: 11,178,202-11,178,331 MTMR9, LOC101929290
    nsv5315252copy number variation1nstd204human GRCh38.p13 chr8: 10,839,055-11,354,546 , GRCh37.p13 chr8: 10,696,565-11,212,055 RPL17P29, SLC35G5, 12 more genes
    nsv5253491copy number variation1nstd204human GRCh38.p13 chr8: 11,300,017-11,329,547 , GRCh37.p13 chr8: 11,157,526-11,187,056 SLC35G5, LOC101929290, 1 more genes
    nsv5247718copy number variation1nstd204human GRCh38.p13 chr8: 10,839,101-11,354,600 , GRCh37.p13 chr8: 10,696,611-11,212,109 TDH, LOC101929290, 12 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4969056copy number variation1nstd200human GRCh38 chr8: 11,172,080-11,973,898 , GRCh37.p13 chr8: 11,029,589-11,831,407 NEIL2, MTMR9, 28 more genes
    nsv4969053copy number variation1nstd200human GRCh38 chr8: 10,839,059-11,354,543 , GRCh37.p13 chr8: 10,696,569-11,212,052 LOC112268022, LOC101929248, 12 more genes
    nsv4959084copy number variation1nstd200human GRCh38 chr8: 11,329,636-11,419,442 , GRCh37.p13 chr8: 11,187,145-11,276,951 SLC35G5, FAM167A-AS1, 5 more genes
    nsv4825617copy number variation1nstd200human GRCh37 chr8: 11,029,589-11,831,407 , GRCh38.p12 chr8: 11,172,080-11,973,898 , GRCh38.p12 chr8|NW_018654717.1: 1,374,123-2,174,821 BLK, TDH-AS1, 28 more genes
    nsv4825615copy number variation1nstd200human GRCh37 chr8: 10,696,569-11,212,052 , GRCh38.p12 chr8: 10,839,059-11,354,543 , GRCh38.p12 chr8|NW_018654717.1: 1,992,308-2,508,204 MTMR9, PINX1, 13 more genes
    nsv4821087copy number variation1nstd200human GRCh37 chr8: 11,187,145-11,276,951 , GRCh38.p12 chr8: 11,329,636-11,419,442 , GRCh38.p12 chr8|NW_018654717.1: 1,929,119-2,017,208 MTMR9, SLC35G5, 6 more genes
    nsv4760008inversion1nstd199human GRCh37 chr8: 7,992,189-12,394,523 , GRCh38.p12 chr8: 8,134,667-12,537,014 , GRCh38.p12 chr8|NW_018654717.1: 1,050,681-5,213,250 , BLK, 129 more genes
    nsv4730173inversion85nstd198human GRCh38 chr8: 7,052,376-12,760,459 , GRCh37.p13 chr8: 6,909,898-12,617,968 , BLK, 214 more genes
    nsv4728933copy number variation1nstd102humanPathogenic GRCh37 chr8: 11,147,024-11,945,856 , GRCh38.p12 chr8: 11,289,515-12,088,347 , GRCh38.p12 chr8|NW_018654717.1: 1,280,656-2,057,334 LOC105379241, DEFB136, 35 more genes
    nsv4685988copy number variation1nstd102humanPathogenic GRCh37 chr8: 161,516-11,516,619 , GRCh38.p12 chr8: 211,516-11,659,110 ZNF705B, RNU6-682P, 232 more genes
    nsv4684267copy number variation1nstd102humanPathogenic GRCh37 chr8: 7,881,478-11,860,845 , GRCh38.p12 chr8|NW_018654717.1: 1,344,700-5,214,290 , GRCh38.p12 chr8: 8,023,956-12,003,336 SUB1P1, DEFB135, 100 more genes
    nsv4675374copy number variation1nstd102humanPathogenic GRCh37 chr8: 8,093,065-11,881,742 , GRCh38.p12 chr8: 8,235,543-12,024,233 , GRCh38.p12 chr8|NW_018654717.1: 1,317,702-5,112,322 PPP1R3B, GATA4, 91 more genes
    nsv4675248copy number variation1nstd102humanPathogenic GRCh37 chr8: 8,093,169-11,936,001 , GRCh38.p12 chr8|NW_018654717.1: 1,280,656-5,112,218 , GRCh38.p12 chr8: 8,235,647-12,078,492 OR7E158P, PPP1R3B, 94 more genes
    nsv4675117copy number variation1nstd102humanPathogenic GRCh37 chr8: 6,999,219-11,895,232 , GRCh38.p12 chr8: 7,141,697-12,037,723 DEFB4B, FAM90A21P, 165 more genes
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