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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970599insertion1nstd209human GRCh38 chr11: 117,924,177-117,924,177 , GRCh37.p13 chr11: 117,794,892-117,794,892 TMPRSS13
    nsv5650043insertion1nstd207human GRCh38 chr11: 117,924,177-117,924,177 , GRCh37.p13 chr11: 117,794,892-117,794,892 TMPRSS13
    nsv5647874insertion2nstd207human GRCh38 chr11: 117,926,048-117,926,048 , GRCh37.p13 chr11: 117,796,763-117,796,763 TMPRSS13
    nsv5601696copy number variation1nstd207human GRCh38 chr11: 117,926,048-117,926,163 , GRCh37.p13 chr11: 117,796,763-117,796,878 TMPRSS13
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5348337translocation1nstd200human GRCh38 chr11: 117,914,050-117,914,050 , GRCh38 chr11: 117,914,156-117,914,156 , GRCh37.p13 chr11: 117,784,871-117,784,871 , GRCh37.p13 chr11: 117,784,765-117,784,765 TMPRSS13
    nsv5331411translocation1nstd200human GRCh37 chr11: 117,784,871-117,784,871 , GRCh37 chr11: 117,784,765-117,784,765 , GRCh38.p12 chr11: 117,914,156-117,914,156 , GRCh38.p12 chr11: 117,914,050-117,914,050 TMPRSS13
    nsv4989346copy number variation1nstd200human GRCh38 chr11: 117,857,085-117,947,830 , GRCh37.p13 chr11: 117,727,800-117,818,545 FXYD6, FXYD6-FXYD2, 1 more genes
    nsv4989345copy number variation1nstd200human GRCh38 chr11: 117,843,046-117,920,750 , GRCh37.p13 chr11: 117,713,761-117,791,465 FXYD6-FXYD2, TMPRSS13, 1 more genes
    nsv4847673copy number variation1nstd200human GRCh37 chr11: 117,713,761-117,791,465 , GRCh38.p12 chr11: 117,843,046-117,920,750 FXYD6, TMPRSS13, 1 more genes
    nsv4767743insertion1nstd199human GRCh37 chr11: 117,794,901-117,794,901 , GRCh38.p12 chr11: 117,924,186-117,924,186 TMPRSS13
    nsv4741952copy number variation1nstd199human GRCh37 chr11: 117,796,842-117,796,958 , GRCh38.p12 chr11: 117,926,127-117,926,243 TMPRSS13
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4349506copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591 LOC107984407, DCPS, 394 more genes
    nsv4349045copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169 MPZL3, ADAMTS8, 393 more genes
    nsv4212369copy number variation1nstd166human GRCh37.p13 chr11: 117,766,924-117,771,574 , GRCh38.p12 chr11: 117,896,209-117,900,859 TMPRSS13
    nsv4210788copy number variation1nstd166human GRCh37.p13 chr11: 117,784,765-117,784,871 , GRCh38.p12 chr11: 117,914,050-117,914,156 TMPRSS13
    nsv4193248copy number variation1nstd166human GRCh37.p13 chr11: 117,786,828-117,787,453 , GRCh38.p12 chr11: 117,916,113-117,916,738 TMPRSS13
    nsv3960881copy number variation1nstd168human GRCh38 chr11: 117,867,827-117,903,272 , GRCh37.p13 chr11: 117,738,542-117,773,987 FXYD6-FXYD2, TMPRSS13, 1 more genes
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