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Items: 1 to 20 of 309

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148239copy number variation1nstd102humanPathogenic GRCh38 chr13: 98,343,655-110,990,677 , GRCh37.p13 chr13: 98,995,909-111,643,024 CLYBL-AS3, PPIAP24, 162 more genes
    nsv7098899copy number variation1nstd102humanPathogenic GRCh37 chr13: 95,675,427-105,286,434 , GRCh38.p12 chr13: 95,023,173-104,634,083 PCCA, LOC105370340, 131 more genes
    nsv7094414copy number variation1nstd102humanPathogenic GRCh37 chr13: 99,336,978-102,379,160 , GRCh38.p12 chr13: 98,684,724-101,726,810 MIR623, UBAC2-AS1, 51 more genes
    nsv7094230copy number variation3nstd102humanUncertain significance GRCh37 chr13: 100,038,233-103,718,599 , GRCh38.p12 chr13: 99,385,979-103,066,249 CLYBL-AS3, LOC107984615, 59 more genes
    nsv7094064copy number variation1nstd102humanUncertain significance GRCh37 chr13: 101,077,867-101,182,420 , GRCh38.p12 chr13: 100,425,613-100,530,166 LOC107984574, RPL7L1P6, 3 more genes
    nsv7093985copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,741,375-101,182,420 , GRCh38.p12 chr13: 100,089,121-100,530,166 PCCA, GGACT, 6 more genes
    nsv7077440inversion1nstd229human GRCh38 chr13: 95,324,680-102,597,006 , GRCh37.p13 chr13: 95,976,934-103,249,356 RN7SL60P, RPL15P18, 111 more genes
    nsv7076855inversion1nstd229human GRCh38 chr13: 100,584,163-100,587,367 , GRCh37.p13 chr13: 101,236,417-101,239,621 GGACT
    nsv7072178inversion1nstd229human GRCh38 chr13: 97,997,035-104,548,310 , GRCh37.p13 chr13: 98,649,289-105,200,661 RNU1-24P, DOCK9, 95 more genes
    nsv7058653inversion1nstd229human GRCh38 chr13: 100,580,727-100,587,515 , GRCh37.p13 chr13: 101,232,981-101,239,769 GGACT
    nsv6957240copy number variation1nstd229human GRCh38 chr13: 100,581,501-100,584,000 , GRCh37.p13 chr13: 101,233,755-101,236,254 GGACT
    nsv6956693copy number variation1nstd229human GRCh38 chr13: 100,558,755-100,586,094 , GRCh37.p13 chr13: 101,211,009-101,238,348 GGACT
    nsv6955184copy number variation1nstd229human GRCh38 chr13: 99,298,801-101,250,600 , GRCh37.p13 chr13: 99,951,055-101,902,951 PCCA-DT, HMGB3P4, 36 more genes
    nsv6953231copy number variation1nstd229human GRCh38 chr13: 100,547,601-100,551,900 , GRCh37.p13 chr13: 101,199,855-101,204,154 GGACT
    nsv6952972copy number variation1nstd229human GRCh38 chr13: 100,524,850-100,528,740 , GRCh37.p13 chr13: 101,177,104-101,180,994 PCCA, GGACT
    nsv6951287copy number variation1nstd229human GRCh38 chr13: 100,516,781-100,623,255 , GRCh37.p13 chr13: 101,169,035-101,275,509 PCCA, GGACT, 3 more genes
    nsv6949334copy number variation1nstd229human GRCh38 chr13: 100,557,025-100,559,249 , GRCh37.p13 chr13: 101,209,279-101,211,503 GGACT
    nsv6948927copy number variation1nstd229human GRCh38 chr13: 100,553,173-100,556,514 , GRCh37.p13 chr13: 101,205,427-101,208,768 GGACT
    nsv6948535copy number variation1nstd229human GRCh38 chr13: 100,580,728-100,584,163 , GRCh37.p13 chr13: 101,232,982-101,236,417 GGACT
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
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