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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093915copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,171,709-111,958,707 , GRCh38.p12 chr11: 111,300,984-112,087,983 CRYAB, BTG4, 34 more genes
    nsv7093830copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,171,709-111,959,745 , GRCh38.p12 chr11: 111,300,984-112,089,021 LOC100132078, DLAT, 34 more genes
    nsv7093669copy number variation2nstd102humanUncertain significance GRCh37 chr11: 111,171,709-112,104,278 , GRCh38.p12 chr11: 111,300,984-112,233,555 CRYAB, RPS6P16, 43 more genes
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    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
    nsv6904968copy number variation1nstd229human GRCh38 chr11: 111,496,095-111,534,266 , GRCh37.p13 chr11: 111,366,820-111,404,991 MIR34C, HOATZ, 3 more genes
    nsv6904289copy number variation1nstd229human GRCh38 chr11: 111,516,864-111,517,062 , GRCh37.p13 chr11: 111,387,589-111,387,787 HOATZ
    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
    nsv6586218inversion1nstd223human GRCh38 chr11: 107,936,497-114,408,912 , GRCh37.p13 chr11: 107,807,223-114,279,634 LOC107984390, ATF4P4, 121 more genes
    nsv6466690copy number variation1nstd223human GRCh38 chr11: 111,525,636-111,526,467 , GRCh37.p13 chr11: 111,396,361-111,397,192 HOATZ
    nsv6464159copy number variation1nstd223human GRCh38 chr11: 111,515,576-111,520,043 , GRCh37.p13 chr11: 111,386,301-111,390,768 HOATZ
    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
    nsv6132342copy number variation1nstd213human GRCh37 chr11: 110,800,000-111,500,001 , GRCh38.p12 chr11: 110,929,276-111,629,277 POU2AF3, POU2AF2, 20 more genes
    nsv5910336copy number variation1nstd209human GRCh38 chr11: 111,520,051-111,527,016 , GRCh37.p13 chr11: 111,390,776-111,397,741 HOATZ
    nsv5850019copy number variation1nstd209human GRCh38 chr11: 111,520,156-111,525,880 , GRCh37.p13 chr11: 111,390,881-111,396,605 HOATZ
    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
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