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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
    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
    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
    nsv6867353copy number variation1nstd229human GRCh38 chr9: 21,226,411-21,239,907 , GRCh37.p13 chr9: 21,226,410-21,239,906 IFNA17, IFNA14, 1 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
    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
    nsv6633716copy number variation2nstd224human GRCh37 chr9: 21,227,670-21,239,850 , GRCh38.p12 chr9: 21,227,671-21,239,851 IFNA14, IFNA17, 1 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
    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
    nsv6562498inversion1nstd223human GRCh38 chr9: 20,655,689-27,693,631 , GRCh37.p13 chr9: 20,655,688-27,693,629 IFNA7, IFNW1, 92 more genes
    nsv6431654copy number variation1nstd223human GRCh38 chr9: 21,240,366-21,254,898 , GRCh37.p13 chr9: 21,240,365-21,254,897 IFNA14
    nsv6430997copy number variation1nstd223human GRCh38 chr9: 21,038,118-21,284,702 , GRCh37.p13 chr9: 21,038,117-21,284,701 IFNWP4, IFNA10, 16 more genes
    nsv6422973copy number variation1nstd223human GRCh38 chr9: 21,205,136-21,237,929 , GRCh37.p13 chr9: 21,205,135-21,237,928 IFNA10, IFNA14, 4 more genes
    nsv6416729copy number variation1nstd223human GRCh38 chr9: 21,225,966-21,237,905 , GRCh37.p13 chr9: 21,225,965-21,237,904 IFNWP5, IFNA17, 1 more genes
    nsv6315463copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-35,903,398 , GRCh38.p12 chr9: 203,861-35,903,401 IFNA11P, RNU6-14P, 495 more genes
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
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