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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069291inversion1nstd229human GRCh38 chr9: 108,067,557-109,076,477 , GRCh37.p13 chr9: 110,829,838-111,838,757 CHCHD4P2, RPL36P14, 14 more genes
    nsv6875677copy number variation1nstd229human GRCh38 chr9: 108,926,658-108,990,571 , GRCh37.p13 chr9: 111,688,938-111,752,851 ELP1, CTNNAL1, 3 more genes
    nsv6874231copy number variation1nstd229human GRCh38 chr9: 108,804,710-109,027,499 , GRCh37.p13 chr9: 111,566,990-111,789,779 LOC100288416, LOC105376216, 8 more genes
    nsv6873163copy number variation1nstd229human GRCh38 chr9: 108,833,288-109,098,702 , GRCh37.p13 chr9: 111,595,568-111,860,982 CTNNAL1, RNA5-8SP3, 8 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
    nsv6632873copy number variation1nstd224human GRCh37 chr9: 111,692,143-111,732,424 , GRCh38.p12 chr9: 108,929,863-108,970,144 ABITRAM, ELP1, 1 more genes
    nsv6564664inversion1nstd223human GRCh38 chr9: 108,945,463-108,946,298 , GRCh37.p13 chr9: 111,707,743-111,708,578 ABITRAM, CTNNAL1
    nsv6454431copy number variation1nstd223human GRCh38 chr9: 108,833,288-109,098,702 , GRCh37.p13 chr9: 111,595,568-111,860,982 TMEM245, MIR32, 8 more genes
    nsv6441594copy number variation1nstd223human GRCh38 chr9: 108,949,392-108,950,640 , GRCh37.p13 chr9: 111,711,672-111,712,920 CTNNAL1, ABITRAM
    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
    nsv6315324copy number variation1nstd102humanPathogenic GRCh37 chr9: 111,644,468-111,696,613 , GRCh38.p12 chr9: 108,882,188-108,934,333 ELP1, ABITRAM
    nsv6314202copy number variation1nstd102humanUncertain significance GRCh37 chr9: 111,560,213-111,984,713 , GRCh38.p12 chr9: 108,797,933-109,222,433 RNU6-984P, LOC105376216, 12 more genes
    nsv6314062copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 109,265,628-117,650,999 , GRCh38.p12 chr9: 106,503,347-114,888,719 ALAD, AMBP, 151 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
    nsv6137428copy number variation1nstd213human GRCh37 chr9: 111,490,000-112,120,001 , GRCh38.p12 chr9: 108,727,720-109,357,721 ELP1, CTNNAL1, 13 more genes
    nsv6137327copy number variation1nstd213human GRCh37 chr9: 109,340,000-112,470,001 , GRCh38.p12 chr9: 106,577,719-109,707,721 ACTL7A, TMEM245, 55 more genes
    nsv6136635copy number variation1nstd213human GRCh37 chr9: 111,410,000-111,850,001 , GRCh38.p12 chr9: 108,647,720-109,087,721 ELP1, CTNNAL1, 9 more genes
    nsv5381738copy number variation1nstd102humanUncertain significance GRCh37 chr9: 111,640,893-111,929,571 , GRCh38.p12 chr9: 108,878,613-109,167,291 LOC105376216, ELP1, 6 more genes
    nsv5301161copy number variation1nstd204human GRCh38.p13 chr9: 108,929,937-108,940,772 , GRCh37.p13 chr9: 111,692,217-111,703,052 ABITRAM, CTNNAL1, 1 more genes
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