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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938068copy number variation1nstd209human GRCh38 chr17: 5,435,768-5,436,757 , GRCh37.p13 chr17: 5,339,088-5,340,077 C1QBP
    nsv5875042copy number variation1nstd209human GRCh38 chr17: 5,435,774-5,436,773 , GRCh37.p13 chr17: 5,339,094-5,340,093 C1QBP
    nsv5594744copy number variation1nstd207human GRCh38 chr17: 5,435,768-5,436,757 , GRCh37.p13 chr17: 5,339,088-5,340,077 C1QBP
    nsv5515585copy number variation1nstd206human GRCh38 chr17: 5,435,818-5,436,748 , GRCh37.p13 chr17: 5,339,138-5,340,068 C1QBP
    nsv5393338copy number variation1nstd186human GRCh37 chr17: 5,339,168-5,340,066 , GRCh38.p12 chr17: 5,435,848-5,436,746 C1QBP
    nsv5393046copy number variation1nstd186human GRCh37 chr17: 5,339,115-5,340,068 , GRCh38.p12 chr17: 5,435,795-5,436,748 C1QBP
    nsv5314619copy number variation1nstd204human GRCh38.p13 chr17: 5,435,815-5,436,757 , GRCh37.p13 chr17: 5,339,135-5,340,077 C1QBP
    nsv5297565copy number variation1nstd204human GRCh38.p13 chr17: 5,436,401-5,488,300 , GRCh37.p13 chr17: 5,339,721-5,391,620 DHX33, MIS12, 3 more genes
    nsv5291561copy number variation1nstd204human GRCh38.p13 chr17: 5,435,774-5,436,773 , GRCh37.p13 chr17: 5,339,094-5,340,093 C1QBP
    nsv5286975copy number variation1nstd204human GRCh38.p13 chr17: 5,435,801-5,436,800 , GRCh37.p13 chr17: 5,339,121-5,340,120 C1QBP
    nsv5193907mobile element insertion1nstd203human GRCh38 chr17: 5,433,977-5,433,997 , GRCh37.p13 chr17: 5,337,297-5,337,317 C1QBP
    nsv5015647copy number variation1nstd200human GRCh38 chr17: 5,435,736-5,436,830 , GRCh37.p13 chr17: 5,339,056-5,340,150 C1QBP
    nsv5015646copy number variation1nstd200human GRCh38 chr17: 5,434,417-5,434,498 , GRCh37.p13 chr17: 5,337,737-5,337,818 C1QBP
    nsv5015645copy number variation1nstd200human GRCh38 chr17: 5,429,920-5,435,917 , GRCh37.p13 chr17: 5,333,240-5,339,237 C1QBP, RPAIN
    nsv5015644copy number variation1nstd200human GRCh38 chr17: 5,429,993-5,431,229 , GRCh37.p13 chr17: 5,333,313-5,334,549 RPAIN, C1QBP
    nsv5015643copy number variation1nstd200human GRCh38 chr17: 5,425,553-5,431,199 , GRCh37.p13 chr17: 5,328,873-5,334,519 C1QBP, RPAIN
    nsv4857860copy number variation1nstd200human GRCh37 chr17: 5,339,168-5,340,067 , GRCh38.p12 chr17: 5,435,848-5,436,747 C1QBP
    nsv4857859copy number variation1nstd200human GRCh37 chr17: 5,337,737-5,337,818 , GRCh38.p12 chr17: 5,434,417-5,434,498 C1QBP
    nsv4857858copy number variation1nstd200human GRCh37 chr17: 5,333,284-5,334,569 , GRCh38.p12 chr17: 5,429,964-5,431,249 RPAIN, C1QBP
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
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