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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969065insertion1nstd209human GRCh38 chr11: 101,938,176-101,938,176 , GRCh37.p13 chr11: 101,808,907-101,808,907 CEP126
    nsv5921598copy number variation1nstd209human GRCh38 chr11: 101,964,045-101,964,371 , GRCh37.p13 chr11: 101,834,776-101,835,102 CEP126
    nsv5730848mobile element insertion1nstd211human GRCh38 chr11: 101,960,809-101,960,809 , GRCh37.p13 chr11: 101,831,540-101,831,540 CEP126
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5654951insertion1nstd207human GRCh38 chr11: 101,925,704-101,925,704 , GRCh37.p13 chr11: 101,796,435-101,796,435 CEP126
    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
    nsv5348224translocation1nstd200human GRCh38 chr11: 101,969,960-101,969,960 , GRCh38 chr11: 101,970,033-101,970,033 , GRCh37.p13 chr11: 101,840,764-101,840,764 , GRCh37.p13 chr11: 101,840,691-101,840,691 CEP126
    nsv5138734mobile element insertion1nstd203human GRCh38 chr11: 101,938,160-101,938,176 , GRCh37.p13 chr11: 101,808,891-101,808,907 CEP126
    nsv5137931mobile element insertion1nstd203human GRCh38 chr11: 101,938,451-101,938,451 , GRCh37.p13 chr11: 101,809,182-101,809,182 CEP126
    nsv5134876mobile element insertion1nstd203human GRCh38 chr11: 101,959,220-101,959,256 , GRCh37.p13 chr11: 101,829,951-101,829,987 CEP126
    nsv5125369mobile element insertion1nstd203human GRCh38 chr11: 101,938,446-101,938,446 , GRCh37.p13 chr11: 101,809,177-101,809,177 CEP126
    nsv5124334mobile element insertion1nstd203human GRCh38 chr11: 101,925,704-101,925,712 , GRCh37.p13 chr11: 101,796,435-101,796,443 CEP126
    nsv5122009mobile element insertion1nstd203human GRCh38 chr11: 101,938,392-101,938,446 , GRCh37.p13 chr11: 101,809,123-101,809,177 CEP126
    nsv5120387mobile element insertion1nstd203human GRCh38 chr11: 101,959,196-101,959,220 , GRCh37.p13 chr11: 101,829,927-101,829,951 CEP126
    nsv4989234copy number variation1nstd200human GRCh38 chr11: 101,565,071-101,983,757 , GRCh37.p13 chr11: 101,435,802-101,854,488 TRPC6, CEP126, 4 more genes
    nsv4980316copy number variation1nstd200human GRCh38 chr11: 101,996,679-102,000,672 , GRCh37.p13 chr11: 101,867,410-101,871,403 CEP126
    nsv4980315copy number variation1nstd200human GRCh38 chr11: 101,935,615-101,943,287 , GRCh37.p13 chr11: 101,806,346-101,814,018 CEP126
    nsv4980314copy number variation1nstd200human GRCh38 chr11: 101,934,314-101,935,821 , GRCh37.p13 chr11: 101,805,045-101,806,552 CEP126
    nsv4846842copy number variation1nstd200human GRCh37 chr11: 101,852,624-101,914,976 , GRCh38.p12 chr11: 101,981,893-102,044,245 CEP126
    nsv4846666copy number variation1nstd200human GRCh37 chr11: 101,805,045-101,806,552 , GRCh38.p12 chr11: 101,934,314-101,935,821 CEP126
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