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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
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7073525inversion1nstd229human GRCh38 chr11: 109,083,255-109,566,663 , GRCh37.p13 chr11: 108,953,982-109,437,389 RNA5SP349, C11orf87
    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
    nsv6909923copy number variation1nstd229human GRCh38 chr11: 108,829,642-109,562,589 , GRCh37.p13 chr11: 108,700,369-109,433,315 RNU6-654P, DDX10, 2 more genes
    nsv6637687copy number variation1nstd102humanPathogenic GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793 GRIA4, MTND1P36, 111 more genes
    nsv6586218inversion1nstd223human GRCh38 chr11: 107,936,497-114,408,912 , GRCh37.p13 chr11: 107,807,223-114,279,634 LOC107984390, ATF4P4, 121 more genes
    nsv6578547inversion1nstd223human GRCh38 chr11: 104,070,004-110,020,477 , GRCh37.p13 chr11: 103,940,732-109,891,203 ACAT1, RNU6-654P, 69 more genes
    nsv6459469copy number variation1nstd223human GRCh38 chr11: 109,420,777-109,421,849 , GRCh37.p13 chr11: 109,291,503-109,292,575 C11orf87
    nsv6458264copy number variation1nstd223human GRCh38 chr11: 109,422,901-109,424,200 , GRCh37.p13 chr11: 109,293,627-109,294,926 C11orf87
    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
    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
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6132072copy number variation1nstd213human GRCh37 chr11: 109,260,000-109,370,001 , GRCh38.p12 chr11: 109,389,274-109,499,275 C11orf87
    nsv6132071copy number variation1nstd213human GRCh37 chr11: 108,670,000-109,310,001 , GRCh38.p12 chr11: 108,799,273-109,439,275 DDX10, CYCSP29, 3 more genes
    nsv5918104copy number variation1nstd209human GRCh38 chr11: 104,190,618-110,044,159 , GRCh37.p13 chr11: 104,061,346-109,914,884 , CARD18, 71 more genes
    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
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5501765copy number variation1nstd206human GRCh38 chr11: 109,427,774-109,427,824 , GRCh37.p13 chr11: 109,298,500-109,298,550 C11orf87
    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
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