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Items: 1 to 20 of 258

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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
    nsv6917689copy number variation1nstd229human GRCh38 chr11: 117,278,754-117,279,089 , GRCh37.p13 chr11: 117,149,470-117,149,805 RNF214
    nsv6910911copy number variation1nstd229human GRCh38 chr11: 117,276,202-117,276,744 , GRCh37.p13 chr11: 117,146,918-117,147,460 RNF214
    nsv6905798copy number variation1nstd229human GRCh38 chr11: 117,256,701-117,264,800 , GRCh37.p13 chr11: 117,127,417-117,135,516 RNF214
    nsv6903393copy number variation1nstd229human GRCh38 chr11: 117,283,016-117,283,246 , GRCh37.p13 chr11: 117,153,732-117,153,962 RNF214, BACE1
    nsv6903106copy number variation1nstd229human GRCh38 chr11: 117,172,701-117,691,700 , GRCh37.p13 chr11: 117,043,417-117,562,415 TAGLN, BACE1, 10 more genes
    nsv6593974inversion1nstd223human GRCh38 chr11: 117,264,834-117,265,471 , GRCh37.p13 chr11: 117,135,550-117,136,187 RNF214
    nsv6580458inversion1nstd223human GRCh38 chr11: 117,247,689-117,248,065 , GRCh37.p13 chr11: 117,118,405-117,118,781 RNF214
    nsv6580245inversion1nstd223human GRCh38 chr11: 117,274,756-117,277,889 , GRCh37.p13 chr11: 117,145,472-117,148,605 RNF214
    nsv6579765inversion1nstd223human GRCh38 chr11: 117,283,654-117,284,805 , GRCh37.p13 chr11: 117,154,370-117,155,521 RNF214, BACE1
    nsv6579484inversion1nstd223human GRCh38 chr11: 114,039,971-117,481,220 , GRCh37.p13 chr11: 113,910,693-117,351,935 RNF214, LOC107984372, 52 more genes
    nsv6474432copy number variation1nstd223human GRCh38 chr11: 117,274,970-117,275,367 , GRCh37.p13 chr11: 117,145,686-117,146,083 RNF214
    nsv6472163copy number variation1nstd223human GRCh38 chr11: 117,252,179-117,252,603 , GRCh37.p13 chr11: 117,122,895-117,123,319 RNF214
    nsv6470079copy number variation1nstd223human GRCh38 chr11: 117,260,874-117,261,794 , GRCh37.p13 chr11: 117,131,590-117,132,510 RNF214
    nsv6465654copy number variation1nstd223human GRCh38 chr11: 117,254,724-117,261,715 , GRCh37.p13 chr11: 117,125,440-117,132,431 RNF214
    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
    nsv6308962copy number variation1nstd102humanUncertain significance GRCh37 chr11: 116,660,844-121,500,272 , GRCh38.p12 chr11: 116,790,128-121,629,563 LOC107984399, PCSK7, 132 more genes
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
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