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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5490124copy number variation1nstd206human GRCh38 chr9: 110,198,561-110,198,768 , GRCh37.p13 chr9: 112,960,841-112,961,048 TRR-TCG6-1, C9orf152
    nsv5315583copy number variation1nstd204human GRCh38.p13 chr9: 109,509,692-110,623,346 , GRCh37.p13 chr9: 112,271,972-113,385,626 TXN, LOC107987013, 13 more genes
    nsv5251857copy number variation1nstd204human GRCh38.p13 chr9: 110,197,092-110,247,950 , GRCh37.p13 chr9: 112,959,372-113,010,230 TXN, TRR-TCG6-1, 1 more genes
    nsv5245704copy number variation1nstd204human GRCh38.p13 chr9: 110,203,541-110,204,940 , GRCh37.p13 chr9: 112,965,821-112,967,220 C9orf152
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4974815copy number variation1nstd200human GRCh38 chr9: 109,983,077-110,215,980 , GRCh37.p13 chr9: 112,745,357-112,978,260 C9orf152, PALM2AKAP2, 3 more genes
    nsv4848078copy number variation1nstd200human GRCh37 chr9: 112,271,976-113,385,617 , GRCh38.p12 chr9: 109,509,696-110,623,337 SVEP1, LOC107987114, 13 more genes
    nsv4847552copy number variation1nstd200human GRCh37 chr9: 112,957,737-112,968,609 , GRCh38.p12 chr9: 110,195,457-110,206,329 TRR-TCG6-1, C9orf152
    nsv4679933copy number variation1nstd189human GRCh37.p13 chr9: 112,934,038-113,196,998 , GRCh38.p12 chr9: 110,171,758-110,434,718 TXN, SVEP1, 7 more genes
    nsv4675980copy number variation1nstd102humanLikely benign GRCh37 chr9: 112,794,010-113,113,206 , GRCh38.p12 chr9: 110,031,730-110,350,926 TXN, LOC107987114, 5 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4415947copy number variation1nstd174human GRCh37 chr9: 112,891,605-113,070,578 , GRCh38.p12 chr9: 110,129,325-110,308,298 TXN, TXNDC8, 5 more genes
    nsv4415712copy number variation1nstd174human GRCh37 chr9: 112,721,869-113,066,303 , GRCh38.p12 chr9: 109,959,589-110,304,023 TXN, TXNDC8, 6 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
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