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Items: 1 to 20 of 324

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137409insertion1nstd232human GRCh37.p13 chr11: 112,202,516-112,202,516 , GRCh38.p12 chr11: 112,331,793-112,331,793 LINC02762
    nsv7076883inversion1nstd229human GRCh38 chr11: 112,279,757-112,290,432 , GRCh37.p13 chr11: 112,150,480-112,161,155 LINC02762
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7072092inversion1nstd229human GRCh38 chr11: 112,292,849-112,293,168 , GRCh37.p13 chr11: 112,163,572-112,163,891 LINC02762
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv7065935inversion1nstd229human GRCh38 chr11: 107,044,115-113,544,291 , GRCh37.p13 chr11: 106,914,841-113,415,013 LINC02762, TIMM8B, 112 more genes
    nsv7060567inversion1nstd229human GRCh38 chr11: 112,292,946-112,297,891 , GRCh37.p13 chr11: 112,163,669-112,168,614 LINC02762
    nsv6917969copy number variation1nstd229human GRCh38 chr11: 112,324,031-112,324,948 , GRCh37.p13 chr11: 112,194,754-112,195,671 LINC02762
    nsv6915759copy number variation1nstd229human GRCh38 chr11: 112,307,101-112,310,600 , GRCh37.p13 chr11: 112,177,824-112,181,323 LINC02762
    nsv6915390copy number variation1nstd229human GRCh38 chr11: 112,361,201-112,366,500 , GRCh37.p13 chr11: 112,231,924-112,237,223 LINC02762
    nsv6912714copy number variation1nstd229human GRCh38 chr11: 112,278,620-112,278,645 , GRCh37.p13 chr11: 112,149,343-112,149,368 LINC02762
    nsv6911137copy number variation1nstd229human GRCh38 chr11: 112,331,777-112,331,915 , GRCh37.p13 chr11: 112,202,500-112,202,638 LINC02762
    nsv6906535copy number variation1nstd229human GRCh38 chr11: 112,271,753-112,299,469 , GRCh37.p13 chr11: 112,142,476-112,170,192 LINC02762
    nsv6904846copy number variation1nstd229human GRCh38 chr11: 112,292,836-112,297,886 , GRCh37.p13 chr11: 112,163,559-112,168,609 LINC02762
    nsv6900902copy number variation1nstd229human GRCh38 chr11: 112,334,657-112,336,475 , GRCh37.p13 chr11: 112,205,380-112,207,198 LINC02762, LOC107984388
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6620697copy number variation1nstd224human GRCh37 chr11: 112,064,216-112,362,462 , GRCh38.p12 chr11: 112,193,493-112,491,739 MRPS36P4, PLET1, 12 more genes
    nsv6620695copy number variation1nstd224human GRCh37 chr11: 111,953,288-112,208,967 , GRCh38.p12 chr11: 112,082,564-112,338,244 TIMM8B, NKAPD1, 15 more genes
    nsv6590314inversion1nstd223human GRCh38 chr11: 112,303,027-112,398,617 , GRCh37.p13 chr11: 112,173,750-112,269,340 LINC02762, RNU6-44P, 1 more genes
    nsv6589533inversion1nstd223human GRCh38 chr11: 112,292,849-112,293,168 , GRCh37.p13 chr11: 112,163,572-112,163,891 LINC02762
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