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Items: 1 to 20 of 523

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957078insertion1nstd209human GRCh38 chr9: 27,219,685-27,219,685 , GRCh37.p13 chr9: 27,219,683-27,219,683 TEK
    nsv5924253copy number variation1nstd209human GRCh38 chr9: 27,119,986-27,126,311 , GRCh37.p13 chr9: 27,119,984-27,126,309 TEK
    nsv5913715copy number variation1nstd209human GRCh38 chr9: 27,137,980-27,138,082 , GRCh37.p13 chr9: 27,137,978-27,138,080 TEK
    nsv5912589copy number variation1nstd209human GRCh38 chr9: 27,194,806-27,296,013 , GRCh37.p13 chr9: 27,194,804-27,296,011 EQTN, RPL36AP34, 3 more genes
    nsv5866741copy number variation1nstd209human GRCh38 chr9: 27,194,071-27,203,824 , GRCh37.p13 chr9: 27,194,069-27,203,822 RNA5SP280, TEK
    nsv5865412copy number variation1nstd209human GRCh38 chr9: 27,203,425-27,205,724 , GRCh37.p13 chr9: 27,203,423-27,205,722 TEK
    nsv5859387copy number variation1nstd209human GRCh38 chr9: 27,221,693-27,225,241 , GRCh37.p13 chr9: 27,221,691-27,225,239 TEK
    nsv5847944copy number variation1nstd209human GRCh38 chr9: 27,120,022-27,126,397 , GRCh37.p13 chr9: 27,120,020-27,126,395 TEK
    nsv5724188mobile element insertion1nstd211human GRCh38 chr9: 27,156,780-27,156,780 , GRCh37.p13 chr9: 27,156,778-27,156,778 TEK
    nsv5717308mobile element insertion1nstd211human GRCh38 chr9: 27,176,274-27,176,274 , GRCh37.p13 chr9: 27,176,272-27,176,272 TEK
    nsv5708424mobile element insertion1nstd211human GRCh38 chr9: 27,181,067-27,181,067 , GRCh37.p13 chr9: 27,181,065-27,181,065 TEK
    nsv5629777insertion1nstd207human GRCh38 chr9: 27,167,377-27,167,377 , GRCh37.p13 chr9: 27,167,375-27,167,375 TEK
    nsv5554317mobile element insertion1nstd206human GRCh38 chr9: 27,156,780-27,156,831 , GRCh37.p13 chr9: 27,156,778-27,156,829 TEK
    nsv5489159copy number variation1nstd206human GRCh38 chr9: 27,118,298-27,122,829 , GRCh37.p13 chr9: 27,118,296-27,122,827 TEK
    nsv5488996copy number variation1nstd206human GRCh38 chr9: 27,194,806-27,296,018 , GRCh37.p13 chr9: 27,194,804-27,296,016 TEK, RPL36AP34, 3 more genes
    nsv5475173copy number variation1nstd206human GRCh38 chr9: 27,221,597-27,222,230 , GRCh37.p13 chr9: 27,221,595-27,222,228 TEK
    nsv5474271copy number variation1nstd206human GRCh38 chr9: 27,138,540-27,139,226 , GRCh37.p13 chr9: 27,138,538-27,139,224 TEK
    nsv5411562mobile element insertion1nstd206human GRCh38 chr9: 27,181,067-27,181,118 , GRCh37.p13 chr9: 27,181,065-27,181,116 TEK
    nsv5372386translocation1nstd200human GRCh38 chr9: 27,155,862-27,155,862 , GRCh38 chr9: 27,171,728-27,171,728 , GRCh37.p13 chr9: 27,155,860-27,155,860 , GRCh37.p13 chr9: 27,171,726-27,171,726 TEK
    nsv5372385translocation1nstd200human GRCh38 chr9: 27,148,056-27,148,056 , GRCh38 chr9: 27,212,616-27,212,616 , GRCh37.p13 chr9: 27,148,054-27,148,054 , GRCh37.p13 chr9: 27,212,614-27,212,614 TEK
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