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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057718inversion1nstd229human GRCh38 chr3: 73,943,893-83,492,461 , GRCh37.p13 chr3: 73,993,044-83,541,612 RN7SL647P, CNTN3, 70 more genes
    nsv7047671inversion1nstd229human GRCh38 chr3: 74,041,567-74,128,729 , GRCh37.p13 chr3: 74,090,718-74,177,880 HSP90AB5P
    nsv7041748inversion1nstd229human GRCh38 chr3: 72,070,390-75,778,215 , GRCh37.p13 chr3: 72,119,541-75,827,366 FTH1P23, LOC107986099, 66 more genes
    nsv7040307inversion1nstd229human GRCh38 chr3: 73,728,944-74,437,847 , GRCh37.p13 chr3: 73,778,095-74,486,998 AKR1B1P2, HSP90AB5P, 3 more genes
    nsv6717967copy number variation1nstd229human GRCh38 chr3: 74,067,391-74,921,684 , GRCh37.p13 chr3: 74,116,542-74,970,835 LOC105377167, HSP90AB5P, 4 more genes
    nsv6714796copy number variation1nstd229human GRCh38 chr3: 74,098,438-74,105,651 , GRCh37.p13 chr3: 74,147,589-74,154,802 HSP90AB5P
    nsv6714552copy number variation1nstd229human GRCh38 chr3: 73,824,901-74,437,800 , GRCh37.p13 chr3: 73,874,052-74,486,951 AKR1B1P2, CNTN3, 3 more genes
    nsv6711295copy number variation1nstd229human GRCh38 chr3: 74,102,759-74,106,400 , GRCh37.p13 chr3: 74,151,910-74,155,551 HSP90AB5P
    nsv6708171copy number variation1nstd229human GRCh38 chr3: 74,097,901-74,105,600 , GRCh37.p13 chr3: 74,147,052-74,154,751 HSP90AB5P
    nsv6705643copy number variation1nstd229human GRCh38 chr3: 74,097,401-74,105,500 , GRCh37.p13 chr3: 74,146,552-74,154,651 HSP90AB5P
    nsv6704212copy number variation1nstd229human GRCh38 chr3: 74,098,401-74,106,700 , GRCh37.p13 chr3: 74,147,552-74,155,851 HSP90AB5P
    nsv6703203copy number variation1nstd229human GRCh38 chr3: 74,099,201-74,105,600 , GRCh37.p13 chr3: 74,148,352-74,154,751 HSP90AB5P
    nsv6628874copy number variation1nstd224human GRCh37 chr3: 74,033,442-74,805,509 , GRCh38.p12 chr3: 73,984,291-74,756,358 HSP90AB5P, AKR1B1P2, 3 more genes
    nsv6554550inversion1nstd223human GRCh38 chr3: 74,041,572-74,128,727 , GRCh37.p13 chr3: 74,090,723-74,177,878 HSP90AB5P
    nsv6365160copy number variation1nstd223human GRCh38 chr3: 74,099,601-74,105,600 , GRCh37.p13 chr3: 74,148,752-74,154,751 HSP90AB5P
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv6134705copy number variation1nstd213human GRCh37 chr3: 66,270,000-87,730,001 , GRCh38.p12 chr3: 66,219,846-87,680,851 , AKR1B1P2, 187 more genes
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5896773copy number variation1nstd209human GRCh38 chr3: 74,098,434-74,105,645 , GRCh37.p13 chr3: 74,147,585-74,154,796 HSP90AB5P
    nsv5837092copy number variation1nstd209human GRCh38 chr3: 74,098,412-74,104,785 , GRCh37.p13 chr3: 74,147,563-74,153,936 HSP90AB5P
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