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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921482copy number variation1nstd209human GRCh38 chr11: 65,300,416-65,300,471 , GRCh37.p13 chr11: 65,067,887-65,067,942 POLA2
    nsv5659665insertion1nstd207human GRCh38 chr11: 65,303,536-65,303,536 , GRCh37.p13 chr11: 65,071,007-65,071,007 POLA2
    nsv5509747copy number variation1nstd206human GRCh38 chr11: 65,304,212-65,304,266 , GRCh37.p13 chr11: 65,071,683-65,071,737 POLA2, LOC105369344
    nsv5501827copy number variation1nstd206human GRCh38 chr11: 65,304,262-65,304,440 , GRCh37.p13 chr11: 65,071,733-65,071,911 POLA2, LOC105369344
    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
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv5128009mobile element insertion1nstd203human GRCh38 chr11: 65,273,170-65,273,170 , GRCh37.p13 chr11: 65,040,641-65,040,641 POLA2
    nsv5122544mobile element insertion1nstd203human GRCh38 chr11: 65,273,165-65,273,170 , GRCh37.p13 chr11: 65,040,636-65,040,641 POLA2
    nsv4985057copy number variation1nstd200human GRCh38 chr11: 65,284,348-65,284,517 , GRCh37.p13 chr11: 65,051,819-65,051,988 POLA2
    nsv4985056copy number variation1nstd200human GRCh38 chr11: 65,270,873-65,284,959 , GRCh37.p13 chr11: 65,038,344-65,052,430 POLA2
    nsv4979834copy number variation1nstd200human GRCh38 chr11: 65,273,692-65,273,908 , GRCh37.p13 chr11: 65,041,163-65,041,379 POLA2
    nsv4979833copy number variation1nstd200human GRCh38 chr11: 65,255,722-65,260,360 , GRCh37.p13 chr11: 65,023,193-65,027,831 POLA2
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4679239copy number variation1nstd189human GRCh37.p13 chr11: 64,222,931-65,140,850 , GRCh38.p12 chr11: 64,455,459-65,373,379 ARL2, VPS51, 52 more genes
    nsv4673085copy number variation1nstd186human GRCh37 chr11: 65,067,397-65,068,169 , GRCh38.p12 chr11: 65,299,926-65,300,698 POLA2
    nsv4600052copy number variation1nstd183human GRCh37 chr11: 65,067,397-65,068,169 , GRCh38.p12 chr11: 65,299,926-65,300,698 POLA2
    nsv4549031insertion1nstd166human GRCh37.p13 chr11: 65,040,636-65,040,636 , GRCh38.p12 chr11: 65,273,165-65,273,165 POLA2
    nsv4478464mobile element insertion1nstd166human GRCh37.p13 chr11: 65,043,763-65,043,763 , GRCh38.p12 chr11: 65,276,292-65,276,292 POLA2
    nsv4436237copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 63,533,279-65,429,676 , GRCh38.p12 chr11: 63,765,807-65,662,205 ARL2, BAD, 117 more genes
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