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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6875616copy number variation1nstd229human GRCh38 chr9: 121,268,701-121,321,400 , GRCh37.p13 chr9: 124,030,979-124,083,678 GSN-AS1, GSN
    nsv6870753copy number variation1nstd229human GRCh38 chr9: 121,243,161-121,300,982 , GRCh37.p13 chr9: 124,005,439-124,063,260 GSN-AS1, GSN
    nsv6864121copy number variation1nstd229human GRCh38 chr9: 121,281,562-121,301,960 , GRCh37.p13 chr9: 124,043,840-124,064,238 GSN-AS1, GSN
    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
    nsv6858984copy number variation1nstd229human GRCh38 chr9: 121,279,653-121,282,197 , GRCh37.p13 chr9: 124,041,931-124,044,475 GSN-AS1, GSN
    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
    nsv6558144inversion1nstd223human GRCh38 chr9: 121,276,195-121,287,426 , GRCh37.p13 chr9: 124,038,473-124,049,704 GSN, GSN-AS1
    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
    nsv6173037copy number variation1nstd214human GRCh38 chr9: 121,283,138-121,283,215 , GRCh37.p13 chr9: 124,045,416-124,045,493 GSN, GSN-AS1
    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
    nsv6004341copy number variation1nstd212human GRCh38 chr9: 121,283,153-121,283,229 , GRCh37.p13 chr9: 124,045,431-124,045,507 GSN-AS1, GSN
    nsv5491819copy number variation1nstd206human GRCh38 chr9: 121,279,041-121,279,112 , GRCh37.p13 chr9: 124,041,319-124,041,390 GSN, GSN-AS1
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4985694copy number variation1nstd200human GRCh38 chr9: 121,243,161-121,300,982 , GRCh37.p13 chr9: 124,005,439-124,063,260 GSN, GSN-AS1
    nsv4842246copy number variation1nstd200human GRCh37 chr9: 124,005,439-124,063,260 , GRCh38.p12 chr9: 121,243,161-121,300,982 GSN-AS1, GSN
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