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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv7075540inversion1nstd229human GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830 S100A11P3, CCND1, 76 more genes
    nsv7073207inversion1nstd229human GRCh38 chr11: 71,538,472-71,581,296 , GRCh37.p13 chr11: 71,249,518-71,292,342 KRTAP5-9, KRTAP5-10, 4 more genes
    nsv6912715copy number variation1nstd229human GRCh38 chr11: 71,563,101-71,654,600 , GRCh37.p13 chr11: 71,274,147-71,365,646 LOC645544, OR7E87P, 6 more genes
    nsv6910508copy number variation1nstd229human GRCh38 chr11: 71,555,699-71,574,106 , GRCh37.p13 chr11: 71,266,745-71,285,152 KRTAP5-13P, KRTAP5-10
    nsv6908275copy number variation1nstd229human GRCh38 chr11: 71,281,500-72,194,614 , GRCh37.p13 chr11: 71,088,949-71,905,658 DEFB130C, ANAPC15, 40 more genes
    nsv6903526copy number variation1nstd229human GRCh38 chr11: 71,559,501-71,571,800 , GRCh37.p13 chr11: 71,270,547-71,282,846 KRTAP5-10, KRTAP5-13P
    nsv6637237copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,051,703-71,655,505 , GRCh38.p12 chr11: 71,340,657-71,944,459 FAM86C1P, KRTAP5-7, 28 more genes
    nsv6459543copy number variation1nstd223human GRCh38 chr11: 71,526,034-71,564,345 , GRCh37.p13 chr11: 71,237,080-71,275,391 KRTAP5-9, KRTAP5-7, 2 more genes
    nsv6458900copy number variation1nstd223human GRCh38 chr11: 71,563,101-71,564,300 , GRCh37.p13 chr11: 71,274,147-71,275,346 KRTAP5-10
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6080947insertion1nstd212human GRCh38 chr11: 71,565,837-71,565,837 , GRCh37.p13 chr11: 71,276,883-71,276,883 KRTAP5-10
    nsv6030035copy number variation1nstd212human GRCh38 chr11: 71,565,826-71,565,975 , GRCh37.p13 chr11: 71,276,872-71,277,021 KRTAP5-10
    nsv5495772copy number variation1nstd206human GRCh38 chr11: 71,525,696-71,565,696 , GRCh37.p13 chr11: 71,236,742-71,276,742 KRTAP5-9, KRTAP5-8, 2 more genes
    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
    nsv5279802copy number variation1nstd204human GRCh38.p13 chr11: 71,563,101-71,564,400 , GRCh37.p13 chr11: 71,274,147-71,275,446 KRTAP5-10
    nsv4681893copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,401-71,907,241 , GRCh38.p12 chr11: 71,435,355-72,196,197 OR7E128P, ZNF705EP, 39 more genes
    nsv4603637copy number variation1nstd183human GRCh37 chr11: 71,274,225-71,275,220 , GRCh38.p12 chr11: 71,563,179-71,564,174 KRTAP5-10
    nsv4360635inversion1nstd169human GRCh37.p13 chr11: 71,275,837-71,294,798 , GRCh38.p12 chr11: 71,564,791-71,583,752 KRTAP5-10, KRTAP5-13P, 2 more genes
    nsv4205093copy number variation1nstd166human GRCh37.p13 chr11: 71,237,543-71,275,844 , GRCh38.p12 chr11: 71,526,497-71,564,798 KRTAP5-10, KRTAP5-7, 2 more genes
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