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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv6876113copy number variation1nstd229human GRCh38 chr9: 21,181,008-21,228,185 , GRCh37.p13 chr9: 21,181,007-21,228,184 IFNA4, IFNA7, 5 more genes
    nsv6873832copy number variation1nstd229human GRCh38 chr9: 20,684,201-21,311,600 , GRCh37.p13 chr9: 20,684,200-21,311,599 IFNWP5, IFNWP18, 22 more genes
    nsv6872666copy number variation1nstd229human GRCh38 chr9: 21,189,138-21,218,660 , GRCh37.p13 chr9: 21,189,137-21,218,659 IFNWP18, IFNA10, 3 more genes
    nsv6871865copy number variation1nstd229human GRCh38 chr9: 21,193,601-21,214,700 , GRCh37.p13 chr9: 21,193,600-21,214,699 IFNA7, IFNWP18, 2 more genes
    nsv6871344copy number variation1nstd229human GRCh38 chr9: 21,215,301-21,227,300 , GRCh37.p13 chr9: 21,215,300-21,227,299 IFNA17, IFNA16
    nsv6869556copy number variation1nstd229human GRCh38 chr9: 21,133,080-21,557,410 , GRCh37.p13 chr9: 21,133,079-21,557,409 IFNWP19, IFNWP2, 27 more genes
    nsv6867511copy number variation1nstd229human GRCh38 chr9: 21,206,598-21,274,027 , GRCh37.p13 chr9: 21,206,597-21,274,026 LOC107987053, IFNA10, 5 more genes
    nsv6865375copy number variation1nstd229human GRCh38 chr9: 21,189,569-21,219,032 , GRCh37.p13 chr9: 21,189,568-21,219,031 IFNWP18, IFNA16, 3 more genes
    nsv6864670copy number variation1nstd229human GRCh38 chr9: 21,038,118-21,284,709 , GRCh37.p13 chr9: 21,038,117-21,284,708 IFNWP18, IFNA17, 16 more genes
    nsv6861059copy number variation1nstd229human GRCh38 chr9: 21,213,847-21,214,499 , GRCh37.p13 chr9: 21,213,846-21,214,498 IFNA16
    nsv6859789copy number variation1nstd229human GRCh38 chr9: 21,213,501-21,214,500 , GRCh37.p13 chr9: 21,213,500-21,214,499 IFNA16
    nsv6637750copy number variation1nstd102humanUncertain significance GRCh37 chr9: 20,659,492-22,347,440 , GRCh38.p12 chr9: 20,659,493-22,347,441 CDKN2B, IFNA10, 46 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
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6633715copy number variation1nstd224human GRCh37 chr9: 21,196,356-21,227,670 , GRCh38.p12 chr9: 21,196,357-21,227,671 IFNA16, IFNA10, 3 more genes
    nsv6633713copy number variation1nstd224human GRCh37 chr9: 21,157,373-21,217,018 , GRCh38.p12 chr9: 21,157,374-21,217,019 IFNA4, IFNA7, 6 more genes
    nsv6633712copy number variation1nstd224human GRCh37 chr9: 21,121,917-21,278,750 , GRCh38.p12 chr9: 21,121,918-21,278,751 IFNA7, IFNA22P, 12 more genes
    nsv6633252copy number variation1nstd224human GRCh37 chr9: 21,201,999-21,214,877 , GRCh38.p12 chr9: 21,202,000-21,214,878 IFNA7, IFNWP18, 2 more genes
    nsv6633251copy number variation1nstd224human GRCh37 chr9: 20,976,421-21,415,687 , GRCh38.p12 chr9: 20,976,422-21,415,688 IFNA5, IFNA16, 27 more genes
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