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Items: 1 to 20 of 290

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951260insertion1nstd209human GRCh38 chr6: 116,135,849-116,135,849 , GRCh37.p13 chr6: 116,457,012-116,457,012 COL10A1, NT5DC1, 1 more genes
    nsv5905586copy number variation1nstd209human GRCh38 chr6: 116,138,517-116,145,394 , GRCh37.p13 chr6: 116,459,680-116,466,557 NT5DC1, COL10A1
    nsv5899571copy number variation1nstd209human GRCh38 chr6: 116,137,246-116,138,492 , GRCh37.p13 chr6: 116,458,409-116,459,655 COL10A1, NT5DC1, 1 more genes
    nsv5844230copy number variation1nstd209human GRCh38 chr6: 116,137,216-116,138,615 , GRCh37.p13 chr6: 116,458,379-116,459,778 NT5DC1, COL10A1, 1 more genes
    nsv5843668copy number variation1nstd209human GRCh38 chr6: 116,138,466-116,145,362 , GRCh37.p13 chr6: 116,459,629-116,466,525 COL10A1, NT5DC1
    nsv5628190insertion1nstd207human GRCh38 chr6: 116,135,847-116,135,847 , GRCh37.p13 chr6: 116,457,010-116,457,010 COL10A1, NT5DC1, 1 more genes
    nsv5548603insertion1nstd206human GRCh38 chr6: 116,135,870-116,135,921 , GRCh37.p13 chr6: 116,457,033-116,457,084 COL10A1, NT5DC1, 1 more genes
    nsv5541419insertion1nstd206human GRCh38 chr6: 116,149,598-116,149,617 , GRCh37.p13 chr6: 116,470,761-116,470,780 COL10A1, NT5DC1
    nsv5535769insertion1nstd206human GRCh38 chr6: 116,135,866-116,135,898 , GRCh37.p13 chr6: 116,457,029-116,457,061 COL10A1, NT5DC1, 1 more genes
    nsv5473858copy number variation1nstd206human GRCh38 chr6: 116,188,354-116,190,478 , GRCh37.p13 chr6: 116,509,517-116,511,641 COL10A1, NT5DC1
    nsv5469958copy number variation1nstd206human GRCh38 chr6: 116,198,593-116,198,952 , GRCh37.p13 chr6: 116,519,756-116,520,115 NT5DC1, COL10A1
    nsv5466199copy number variation1nstd206human GRCh38 chr6: 116,172,370-116,172,467 , GRCh37.p13 chr6: 116,493,533-116,493,630 NT5DC1, COL10A1
    nsv5465230copy number variation1nstd206human GRCh38 chr6: 116,121,762-116,121,836 , GRCh37.p13 chr6: 116,442,925-116,442,999 NT5DC1, COL10A1
    nsv5458177copy number variation1nstd206human GRCh38 chr6: 116,138,517-116,145,395 , GRCh37.p13 chr6: 116,459,680-116,466,558 NT5DC1, COL10A1
    nsv5455193copy number variation1nstd206human GRCh38 chr6: 116,165,098-116,166,185 , GRCh37.p13 chr6: 116,486,261-116,487,348 COL10A1, NT5DC1
    nsv5369654translocation1nstd200human GRCh38 chr6: 116,138,517-116,138,517 , GRCh38 chr6: 116,145,395-116,145,395 , GRCh37.p13 chr6: 116,466,558-116,466,558 , GRCh37.p13 chr6: 116,459,680-116,459,680 NT5DC1, COL10A1
    nsv5310972copy number variation1nstd204human GRCh37.p13 chr6: 116,459,657-116,466,580 , GRCh38.p13 chr6: 116,138,494-116,145,417 COL10A1, NT5DC1
    nsv5235049copy number variation1nstd204human GRCh38.p13 chr6: 116,138,501-116,145,400 , GRCh37.p13 chr6: 116,459,664-116,466,563 NT5DC1, COL10A1
    nsv5223496copy number variation1nstd204human GRCh38.p13 chr6: 116,120,501-116,122,000 , GRCh37.p13 chr6: 116,441,664-116,443,163 NT5DC1, COL10A1
    nsv5220531copy number variation1nstd204human GRCh38.p13 chr6: 116,138,466-116,145,437 , GRCh37.p13 chr6: 116,459,629-116,466,600 COL10A1, NT5DC1
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