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Items: 1 to 20 of 334

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926561copy number variation1nstd209human GRCh38 chr10: 79,825,669-87,341,680 , GRCh37.p13 chr10: 81,585,425-89,101,437 , RPL12P29, 110 more genes
    nsv5913599copy number variation1nstd209human GRCh38 chr10: 80,482,350-80,482,798 , GRCh37.p13 chr10: 82,242,106-82,242,554 TSPAN14
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5696231mobile element insertion1nstd211human GRCh38 chr10: 80,491,874-80,491,874 , GRCh37.p13 chr10: 82,251,630-82,251,630 TSPAN14
    nsv5627000insertion1nstd207human GRCh38 chr10: 80,533,272-80,533,272 , GRCh37.p13 chr10: 82,293,028-82,293,028 TSPAN14, TSPAN14-AS1
    nsv5590635copy number variation1nstd207human GRCh38 chr10: 80,482,350-80,482,798 , GRCh37.p13 chr10: 82,242,106-82,242,554 TSPAN14
    nsv5486036copy number variation1nstd206human GRCh38 chr10: 80,482,369-80,482,821 , GRCh37.p13 chr10: 82,242,125-82,242,577 TSPAN14
    nsv5409018mobile element insertion1nstd206human GRCh38 chr10: 80,491,874-80,491,925 , GRCh37.p13 chr10: 82,251,630-82,251,681 TSPAN14
    nsv5388923copy number variation1nstd186human GRCh37 chr10: 82,242,102-82,242,382 , GRCh38.p12 chr10: 80,482,346-80,482,626 TSPAN14
    nsv5386085copy number variation1nstd186human GRCh37 chr10: 82,242,175-82,242,496 , GRCh38.p12 chr10: 80,482,419-80,482,740 TSPAN14
    nsv5385938copy number variation1nstd186human GRCh37 chr10: 82,242,117-82,242,533 , GRCh38.p12 chr10: 80,482,361-80,482,777 TSPAN14
    nsv5383358mobile element deletion1nstd186human GRCh37 chr10: 82,242,482-82,242,793 , GRCh38.p12 chr10: 80,482,726-80,483,037 TSPAN14
    nsv5313298copy number variation1nstd204human GRCh38.p13 chr10: 80,468,242-80,468,997 , GRCh37.p13 chr10: 82,227,998-82,228,753 TSPAN14
    nsv5306864copy number variation1nstd204human GRCh38.p13 chr10: 80,452,728-80,679,432 , GRCh37.p13 chr10: 82,212,484-82,439,188 TSPAN14-AS1, SH2D4B, 3 more genes
    nsv5301788copy number variation1nstd204human GRCh38.p13 chr10: 80,482,338-80,482,780 , GRCh37.p13 chr10: 82,242,094-82,242,536 TSPAN14
    nsv5255766copy number variation1nstd204human GRCh38.p13 chr10: 80,455,901-80,483,700 , GRCh37.p13 chr10: 82,215,657-82,243,456 TSPAN14
    nsv5249792copy number variation1nstd204human GRCh38.p13 chr10: 80,502,206-80,525,085 , GRCh37.p13 chr10: 82,261,962-82,284,841 TSPAN14
    nsv5246345copy number variation1nstd204human GRCh38.p13 chr10: 80,452,708-80,482,083 , GRCh37.p13 chr10: 82,212,464-82,241,839 TSPAN14
    nsv5246279copy number variation1nstd204human GRCh38.p13 chr10: 80,533,301-80,536,000 , GRCh37.p13 chr10: 82,293,057-82,295,756 SH2D4B, TSPAN14-AS1, 1 more genes
    nsv5245880copy number variation1nstd204human GRCh38.p13 chr10: 80,483,901-80,688,900 , GRCh37.p13 chr10: 82,243,657-82,448,656 SH2D4B, TSPAN14-AS1, 3 more genes
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