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Items: 1 to 20 of 305

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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
    nsv7141562insertion1nstd232human GRCh37.p13 chr8: 27,680,006-27,680,006 , GRCh38.p12 chr8: 27,822,489-27,822,489 PBK
    nsv7061563inversion1nstd229human GRCh38 chr8: 27,492,341-29,312,113 , GRCh37.p13 chr8: 27,349,858-29,169,630 LOC100130612, HMBOX1, 37 more genes
    nsv6856263copy number variation1nstd229human GRCh38 chr8: 27,818,356-27,819,268 , GRCh37.p13 chr8: 27,675,873-27,676,785 PBK
    nsv6853493copy number variation1nstd229human GRCh38 chr8: 27,802,596-27,809,897 , GRCh37.p13 chr8: 27,660,113-27,667,414 ESCO2, PBK
    nsv6851044copy number variation1nstd229human GRCh38 chr8: 27,826,801-27,922,100 , GRCh37.p13 chr8: 27,684,318-27,779,617 SCARA5, PBK, 3 more genes
    nsv6851033copy number variation1nstd229human GRCh38 chr8: 27,819,190-27,875,057 , GRCh37.p13 chr8: 27,676,707-27,732,574 PBK, LOC100130612, 1 more genes
    nsv6850406copy number variation1nstd229human GRCh38 chr8: 27,823,274-27,831,032 , GRCh37.p13 chr8: 27,680,791-27,688,549 PBK
    nsv6843243copy number variation1nstd229human GRCh38 chr8: 27,817,394-27,817,578 , GRCh37.p13 chr8: 27,674,911-27,675,095 PBK
    nsv6841799copy number variation1nstd229human GRCh38 chr8: 27,826,528-27,826,814 , GRCh37.p13 chr8: 27,684,045-27,684,331 PBK
    nsv6839948copy number variation1nstd229human GRCh38 chr8: 27,828,701-27,863,200 , GRCh37.p13 chr8: 27,686,218-27,720,717 LOC100130612, PBK
    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
    nsv6635576copy number variation1nstd227human GRCh38.p12 chr8: 27,823,059-27,844,936 , GRCh37 chr8: 27,680,576-27,702,453 PBK, LOC100130612
    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
    nsv6563623inversion1nstd223human GRCh38 chr8: 27,834,847-27,835,697 , GRCh37.p13 chr8: 27,692,364-27,693,214 PBK
    nsv6559852inversion1nstd223human GRCh38 chr8: 27,833,435-27,834,123 , GRCh37.p13 chr8: 27,690,952-27,691,640 PBK
    nsv6559713inversion1nstd223human GRCh38 chr8: 27,833,691-27,834,620 , GRCh37.p13 chr8: 27,691,208-27,692,137 PBK
    nsv6559209inversion1nstd223human GRCh38 chr8: 27,833,404-27,834,002 , GRCh37.p13 chr8: 27,690,921-27,691,519 PBK
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