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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6876468copy number variation1nstd229human GRCh38 chr9: 121,363,250-121,363,385 , GRCh37.p13 chr9: 124,125,528-124,125,663 STOM
    nsv6872277copy number variation1nstd229human GRCh38 chr9: 121,339,301-121,361,300 , GRCh37.p13 chr9: 124,101,579-124,123,578 STOM
    nsv6865276copy number variation1nstd229human GRCh38 chr9: 121,286,039-121,366,075 , GRCh37.p13 chr9: 124,048,317-124,128,353 GSN, STOM
    nsv6863361copy number variation1nstd229human GRCh38 chr9: 121,361,328-121,363,439 , GRCh37.p13 chr9: 124,123,606-124,125,717 STOM
    nsv6860580copy number variation1nstd229human GRCh38 chr9: 121,253,488-121,755,032 , GRCh37.p13 chr9: 124,015,766-124,517,311 RN7SL187P, GGTA1, 8 more genes
    nsv6860161copy number variation1nstd229human GRCh38 chr9: 121,341,410-121,348,012 , GRCh37.p13 chr9: 124,103,688-124,110,290 STOM
    nsv6860071copy number variation1nstd229human GRCh38 chr9: 121,334,918-121,344,235 , GRCh37.p13 chr9: 124,097,196-124,106,513 STOM
    nsv6859894copy number variation1nstd229human GRCh38 chr9: 121,361,329-121,363,436 , GRCh37.p13 chr9: 124,123,607-124,125,714 STOM
    nsv6637981copy number variation1nstd102humanPathogenic GRCh37 chr9: 124,018,736-129,995,568 , GRCh38.p12 chr9: 121,256,458-127,233,289 PBX3-DT, ADGRD2, 119 more genes
    nsv6637716copy number variation1nstd102humanUncertain significance GRCh37 chr9: 124,024,959-124,157,971 , GRCh38.p12 chr9: 121,262,681-121,395,693 GSN, GSN-AS1, 2 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633663copy number variation1nstd224human GRCh37 chr9: 124,060,879-124,125,324 , GRCh38.p12 chr9: 121,298,601-121,363,046 STOM, GSN
    nsv6451657copy number variation1nstd223human GRCh38 chr9: 121,361,328-121,363,435 , GRCh37.p13 chr9: 124,123,606-124,125,713 STOM
    nsv6446468copy number variation1nstd223human GRCh38 chr9: 121,365,106-121,365,517 , GRCh37.p13 chr9: 124,127,384-124,127,795 STOM
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291398copy number variation1nstd102humanPathogenic GRCh37 chr9: 120,045,175-127,335,905 , GRCh38.p12 chr9: 117,282,896-124,573,626 ZBTB6, LOC105376253, 107 more genes
    nsv6290238copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,853,848-124,633,077 , GRCh38.p12 chr9: 115,091,569-121,870,798 LINC00474, LOC107987123, 72 more genes
    nsv6137052copy number variation1nstd213human GRCh37 chr9: 123,200,000-125,840,001 , GRCh38.p12 chr9: 120,437,722-123,077,722 MEGF9, GGTA1, 61 more genes
    nsv5373067translocation1nstd200human GRCh38 chr9: 121,363,435-121,363,435 , GRCh38 chr9: 121,361,328-121,361,328 , GRCh37.p13 chr9: 124,123,606-124,123,606 , GRCh37.p13 chr9: 124,125,713-124,125,713 STOM
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