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Items: 1 to 20 of 3192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112759copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,001-8,472,742 , GRCh38.p12 chr3: 18,324-8,431,056 LOC105376926, LOC107986057, 69 more genes
    nsv5976979inversion1nstd209human GRCh38 chr3: 2,423,934-2,424,225 , GRCh37.p13 chr3: 2,465,618-2,465,909 CNTN4
    nsv5966910insertion1nstd209human GRCh38 chr3: 2,611,312-2,611,312 , GRCh37.p13 chr3: 2,652,996-2,652,996 CNTN4
    nsv5966041insertion1nstd209human GRCh38 chr3: 2,920,310-2,920,310 , GRCh37.p13 chr3: 2,961,994-2,961,994 CNTN4
    nsv5966033insertion1nstd209human GRCh38 chr3: 2,746,094-2,746,094 , GRCh37.p13 chr3: 2,787,778-2,787,778 CNTN4
    nsv5965741insertion1nstd209human GRCh38 chr3: 2,129,413-2,129,413 , GRCh37.p13 chr3: 2,171,097-2,171,097 CNTN4-AS2, CNTN4
    nsv5962935insertion1nstd209human GRCh38 chr3: 2,222,582-2,222,582 , GRCh37.p13 chr3: 2,264,266-2,264,266 CNTN4
    nsv5958745insertion1nstd209human GRCh38 chr3: 2,772,347-2,772,347 , GRCh37.p13 chr3: 2,814,031-2,814,031 CNTN4
    nsv5952006insertion1nstd209human GRCh38 chr3: 2,340,705-2,340,705 , GRCh37.p13 chr3: 2,382,389-2,382,389 CNTN4
    nsv5951994insertion1nstd209human GRCh38 chr3: 2,499,753-2,499,753 , GRCh37.p13 chr3: 2,541,437-2,541,437 CNTN4
    nsv5950551insertion1nstd209human GRCh38 chr3: 2,481,025-2,481,025 , GRCh37.p13 chr3: 2,522,709-2,522,709 CNTN4
    nsv5949367insertion1nstd209human GRCh38 chr3: 2,834,898-2,834,898 , GRCh37.p13 chr3: 2,876,582-2,876,582 LOC105376926, CNTN4
    nsv5949301insertion1nstd209human GRCh38 chr3: 2,841,849-2,841,849 , GRCh37.p13 chr3: 2,883,533-2,883,533 LOC105376926, CNTN4
    nsv5907284copy number variation1nstd209human GRCh38 chr3: 2,316,750-2,318,061 , GRCh37.p13 chr3: 2,358,434-2,359,745 CNTN4
    nsv5904332copy number variation1nstd209human GRCh38 chr3: 2,427,648-2,428,007 , GRCh37.p13 chr3: 2,469,332-2,469,691 CNTN4
    nsv5903919copy number variation1nstd209human GRCh38 chr3: 2,263,830-2,270,748 , GRCh37.p13 chr3: 2,305,514-2,312,432 CNTN4
    nsv5903626copy number variation1nstd209human GRCh38 chr3: 2,741,314-2,743,885 , GRCh37.p13 chr3: 2,782,998-2,785,569 CNTN4
    nsv5903579copy number variation1nstd209human GRCh38 chr3: 2,263,846-2,271,089 , GRCh37.p13 chr3: 2,305,530-2,312,773 CNTN4
    nsv5903185copy number variation1nstd209human GRCh38 chr3: 2,306,761-2,307,331 , GRCh37.p13 chr3: 2,348,445-2,349,015 CNTN4
    nsv5901969copy number variation1nstd209human GRCh38 chr3: 2,544,145-2,565,654 , GRCh37.p13 chr3: 2,585,829-2,607,338 CNTN4
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