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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070278inversion1nstd229human GRCh38 chr9: 85,364,427-88,288,635 , GRCh37.p13 chr9: 87,979,342-90,903,550 LOC105376121, CTSL3P, 57 more genes
    nsv7070039inversion1nstd229human GRCh38 chr9: 87,255,950-90,941,993 , GRCh37.p13 chr9: 89,870,865-93,704,275 LOC389768, RPS10P3, 69 more genes
    nsv7068881inversion1nstd229human GRCh38 chr9: 85,364,378-88,276,332 , GRCh37.p13 chr9: 87,979,293-90,891,247 LOC100129202, LOC100287212, 57 more genes
    nsv7066485inversion1nstd229human GRCh38 chr9: 87,915,480-88,146,042 , GRCh37.p13 chr9: 90,530,395-90,760,957 LOC497256, RPS10P3, 8 more genes
    nsv7063033inversion1nstd229human GRCh38 chr9: 87,919,277-88,133,682 , GRCh37.p13 chr9: 90,534,192-90,748,597 CDK20, RPS10P3, 7 more genes
    nsv7062112inversion1nstd229human GRCh38 chr9: 87,932,613-88,115,079 , GRCh37.p13 chr9: 90,547,528-90,729,994 LOC497256, LOC105376131, 5 more genes
    nsv7059923inversion1nstd229human GRCh38 chr9: 87,301,614-87,977,114 , GRCh37.p13 chr9: 89,916,529-90,592,029 CTSL, LOC105376131, 21 more genes
    nsv6876414copy number variation1nstd229human GRCh38 chr9: 87,623,057-88,194,238 , GRCh37.p13 chr9: 90,237,972-90,809,153 DAPK1, RNU6-86P, 24 more genes
    nsv6865419copy number variation1nstd229human GRCh38 chr9: 87,901,901-88,717,300 , GRCh37.p13 chr9: 90,516,816-91,332,215 LOC100129202, RNU6-86P, 18 more genes
    nsv6862777copy number variation1nstd229human GRCh38 chr9: 86,566,451-88,481,061 , GRCh37.p13 chr9: 89,181,366-91,095,976 CTSL3P, CTSLP8, 40 more genes
    nsv6637616copy number variation1nstd102humanUncertain significance GRCh37 chr9: 90,266,171-90,565,780 , GRCh38.p12 chr9: 87,651,256-87,950,865 FBP2P1, SPATA31C1, 15 more genes
    nsv6634980copy number variation1nstd227human GRCh38.p12 chr9: 87,900,704-88,081,422 , GRCh37 chr9: 90,515,619-90,696,337 CDK20, RPS10P3, 6 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
    nsv6561881inversion1nstd223human GRCh38 chr9: 87,912,735-88,136,103 , GRCh37.p13 chr9: 90,527,650-90,751,018 CDK20, RPS10P3, 7 more genes
    nsv6452965copy number variation1nstd223human GRCh38 chr9: 87,940,901-87,944,800 , GRCh37.p13 chr9: 90,555,816-90,559,715 LOC645937
    nsv6442427copy number variation1nstd223human GRCh38 chr9: 87,877,508-88,019,562 , GRCh37.p13 chr9: 90,492,423-90,634,477 LOC645937, RNU6-86P, 6 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
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 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
    nsv6291242copy number variation1nstd102humanUncertain significance GRCh37 chr9: 90,336,741-90,609,494 , GRCh38.p12 chr9: 87,721,826-87,994,579 NPAP1P7, CTSL3P, 16 more genes
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