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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6877500copy number variation1nstd229human GRCh38 chr9: 110,195,461-110,206,330 , GRCh37.p13 chr9: 112,957,741-112,968,610 C9orf152, TRR-TCG6-1
    nsv6865713copy number variation1nstd229human GRCh38 chr9: 109,983,077-110,215,980 , GRCh37.p13 chr9: 112,745,357-112,978,260 PALM2AKAP2, RPL21P87, 3 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
    nsv6633386copy number variation1nstd224human GRCh37 chr9: 112,891,853-112,970,634 , GRCh38.p12 chr9: 110,129,573-110,208,354 LOC105376217, C9orf152, 2 more genes
    nsv6441527copy number variation1nstd223human GRCh38 chr9: 110,190,601-110,309,700 , GRCh37.p13 chr9: 112,952,881-113,071,980 C9orf152, TXN, 3 more genes
    nsv6441393copy number variation1nstd223human GRCh38 chr9: 109,983,077-110,215,980 , GRCh37.p13 chr9: 112,745,357-112,978,260 LOC105376217, RPL21P87, 3 more genes
    nsv6437552copy number variation1nstd223human GRCh38 chr9: 110,159,107-110,309,502 , GRCh37.p13 chr9: 112,921,387-113,071,782 TXN, TXNDC8, 5 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
    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
    nsv6137429copy number variation1nstd213human GRCh37 chr9: 112,870,000-113,510,001 , GRCh38.p12 chr9: 110,107,720-110,747,721 MUSK, TXN, 10 more genes
    nsv6136723copy number variation1nstd213human GRCh37 chr9: 112,800,000-113,050,001 , GRCh38.p12 chr9: 110,037,720-110,287,721 TXN, C9orf152, 4 more genes
    nsv6136638copy number variation1nstd213human GRCh37 chr9: 112,970,000-113,120,001 , GRCh38.p12 chr9: 110,207,720-110,357,721 TXN, TXNDC8, 2 more genes
    nsv6136637copy number variation1nstd213human GRCh37 chr9: 112,600,000-112,970,001 , GRCh38.p12 chr9: 109,837,720-110,207,721 C9orf152, PALM2AKAP2, 3 more genes
    nsv5966241insertion1nstd209human GRCh38 chr9: 110,198,893-110,198,893 , GRCh37.p13 chr9: 112,961,173-112,961,173 TRR-TCG6-1, C9orf152
    nsv5911341copy number variation1nstd209human GRCh38 chr9: 110,195,457-110,206,328 , GRCh37.p13 chr9: 112,957,737-112,968,608 C9orf152, TRR-TCG6-1
    nsv5857525copy number variation1nstd209human GRCh38 chr9: 110,204,241-110,206,340 , GRCh37.p13 chr9: 112,966,521-112,968,620 C9orf152
    nsv5856428copy number variation1nstd209human GRCh38 chr9: 110,195,692-110,206,240 , GRCh37.p13 chr9: 112,957,972-112,968,520 TRR-TCG6-1, C9orf152
    nsv5491597copy number variation1nstd206human GRCh38 chr9: 109,959,589-110,304,026 , GRCh37.p13 chr9: 112,721,869-113,066,306 TXN, TXNDC8, 6 more genes
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