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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066656inversion1nstd229human GRCh38 chr17: 40,822,205-41,582,529 , GRCh37.p13 chr17: 38,978,457-39,738,781 LOC105371777, KRT10, 69 more genes
    nsv6987154copy number variation1nstd229human GRCh38 chr17: 41,277,005-41,430,682 , GRCh37.p13 chr17|NW_003315953.1: 16,589-119,548 , GRCh37.p13 chr17: 39,433,257-39,586,934 TBC1D3P7, KRT41P, 11 more genes
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6983380copy number variation1nstd229human GRCh38 chr17: 41,420,011-41,420,170 , GRCh37.p13 chr17: 39,576,263-39,576,422 KRT37
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6504427copy number variation1nstd223human GRCh38 chr17: 41,277,005-41,430,682 , GRCh37.p13 chr17|NW_003315953.1: 16,589-119,548 , GRCh37.p13 chr17: 39,433,257-39,586,934 KRTAP16-1, TBC1D3P7, 11 more genes
    nsv6498137copy number variation1nstd223human GRCh38 chr17: 41,422,708-41,439,319 , GRCh37.p13 chr17: 39,578,960-39,595,571 KRT38, KRT37
    nsv6133056copy number variation1nstd213human GRCh37 chr17: 36,400,000-39,740,001 , GRCh38.p12 chr17: 38,545,381-41,583,749 CACNB1, CDC6, 176 more genes
    nsv5556761sequence alteration1nstd206human GRCh38 chr17: 41,422,593-41,422,807 , GRCh37.p13 chr17: 39,578,845-39,579,059 KRT37
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5297588copy number variation1nstd204human GRCh38.p13 chr17: 41,423,701-41,428,000 , GRCh37.p13 chr17: 39,579,953-39,584,252 KRT37
    nsv5016377copy number variation1nstd200human GRCh38 chr17: 41,420,298-41,420,368 , GRCh37.p13 chr17: 39,576,550-39,576,620 KRT37
    nsv5013700copy number variation1nstd200human GRCh38 chr17: 41,277,005-41,430,685 , GRCh37.p13 chr17|NW_003315953.1: 16,589-119,548 , GRCh37.p13 chr17: 39,433,257-39,586,937 KRT37, LOC105371778, 11 more genes
    nsv4858821copy number variation1nstd200human GRCh37 chr17: 39,582,298-39,584,303 , GRCh38.p12 chr17: 41,426,046-41,428,051 , GRCh38.p12 chr17|NW_003315953.2: 4,885-6,890 KRT37
    nsv4680071copy number variation1nstd189human GRCh37.p13 chr17: 39,432,725-40,293,644 , GRCh38.p12 chr17: 41,276,473-42,141,626 ACLY, CNP, 50 more genes
    nsv4670387copy number variation1nstd186human GRCh37 chr17: 39,582,296-39,584,303 , GRCh38.p12 chr17|NW_003315953.2: 4,885-6,892 , GRCh38.p12 chr17: 41,426,044-41,428,051 KRT37
    nsv4645397copy number variation4nstd186human GRCh37 chr17: 39,582,298-39,584,303 , GRCh38.p12 chr17|NW_003315953.2: 4,885-6,890 , GRCh38.p12 chr17: 41,426,046-41,428,051 KRT37
    nsv4645299copy number variation1nstd186human GRCh37 chr17: 39,582,294-39,584,308 , GRCh38.p12 chr17|NW_003315953.2: 4,880-6,894 , GRCh38.p12 chr17: 41,426,042-41,428,056 KRT37
    nsv4624753copy number variation1nstd183human GRCh37 chr17: 39,581,298-39,594,809 , GRCh38.p12 chr17: 41,425,046-41,438,557 , GRCh38.p12 chr17|NW_003315953.2: 1-7,890 KRT37, KRT38
    nsv4622340copy number variation1nstd183human GRCh37 chr17: 39,582,296-39,584,303 , GRCh38.p12 chr17: 41,426,044-41,428,051 , GRCh38.p12 chr17|NW_003315953.2: 4,885-6,892 KRT37
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