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Items: 1 to 20 of 926

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093918copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 116,660,844-117,870,356 , GRCh38.p12 chr11: 116,790,128-117,999,641 PAFAH1B2, FXYD2, 26 more genes
    nsv7093833copy number variation6nstd102humanUncertain significance GRCh37 chr11: 116,691,583-121,500,272 , GRCh38.p12 chr11: 116,820,867-121,629,563 RN7SL688P, MIR4492, 131 more genes
    nsv7093753copy number variation1nstd102humanUncertain significance GRCh37 chr11: 117,209,303-120,133,495 , GRCh38.p12 chr11: 117,338,587-120,262,786 TMEM25, HYOU1, 93 more genes
    nsv7070633inversion1nstd229human GRCh38 chr11: 117,651,143-117,658,375 , GRCh37.p13 chr11: 117,521,858-117,529,090 DSCAML1, LOC105369515
    nsv7068897inversion1nstd229human GRCh38 chr11: 117,654,332-117,658,199 , GRCh37.p13 chr11: 117,525,047-117,528,914 LOC105369515, DSCAML1
    nsv7068043inversion1nstd229human GRCh38 chr11: 117,677,693-117,680,522 , GRCh37.p13 chr11: 117,548,408-117,551,237 DSCAML1
    nsv7062420inversion1nstd229human GRCh38 chr11: 117,681,463-119,526,734 , GRCh37.p13 chr11: 117,552,178-119,397,444 RN7SL688P, MIR4492, 72 more genes
    nsv6916849copy number variation1nstd229human GRCh38 chr11: 117,685,096-117,687,988 , GRCh37.p13 chr11: 117,555,811-117,558,703 DSCAML1
    nsv6916832copy number variation1nstd229human GRCh38 chr11: 117,525,796-117,530,323 , GRCh37.p13 chr11: 117,396,511-117,401,038 DSCAML1
    nsv6915779copy number variation1nstd229human GRCh38 chr11: 117,555,531-117,559,895 , GRCh37.p13 chr11: 117,426,246-117,430,610 DSCAML1
    nsv6915544copy number variation1nstd229human GRCh38 chr11: 117,686,142-117,688,159 , GRCh37.p13 chr11: 117,556,857-117,558,874 DSCAML1
    nsv6914223copy number variation1nstd229human GRCh38 chr11: 117,409,240-117,450,025 , GRCh37.p13 chr11: 117,279,956-117,320,741 DSCAML1, CEP164
    nsv6913362copy number variation1nstd229human GRCh38 chr11: 117,676,711-117,680,522 , GRCh37.p13 chr11: 117,547,426-117,551,237 DSCAML1
    nsv6913051copy number variation1nstd229human GRCh38 chr11: 117,816,019-117,818,525 , GRCh37.p13 chr11: 117,686,734-117,689,240 FXYD2, DSCAML1, 1 more genes
    nsv6912689copy number variation1nstd229human GRCh38 chr11: 117,658,091-117,671,802 , GRCh37.p13 chr11: 117,528,806-117,542,517 LOC105369515, DSCAML1
    nsv6912471copy number variation1nstd229human GRCh38 chr11: 117,498,508-117,502,711 , GRCh37.p13 chr11: 117,369,223-117,373,426 DSCAML1
    nsv6911848copy number variation1nstd229human GRCh38 chr11: 117,377,701-117,555,700 , GRCh37.p13 chr11: 117,248,417-117,426,415 DSCAML1, CEP164
    nsv6911773copy number variation1nstd229human GRCh38 chr11: 117,505,247-117,505,624 , GRCh37.p13 chr11: 117,375,962-117,376,339 DSCAML1
    nsv6911154copy number variation1nstd229human GRCh38 chr11: 117,761,739-117,765,219 , GRCh37.p13 chr11: 117,632,454-117,635,934 DSCAML1
    nsv6911014copy number variation1nstd229human GRCh38 chr11: 117,391,201-117,556,500 , GRCh37.p13 chr11: 117,261,917-117,427,215 CEP164, DSCAML1
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