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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148164copy number variation1nstd102humanPathogenic GRCh38 chr13: 106,425,676-114,326,445 , GRCh37.p13 chr13: 107,078,024-115,085,141 TUBGCP3, LINC01043, 132 more genes
    nsv7145250copy number variation1nstd232human GRCh37.p13 chr13: 113,062,843-113,062,891 , GRCh38.p12 chr13: 112,408,529-112,408,577 , GRCh38.p12 chr13|NT_187592.1: 209,499-209,547 SPACA7, LOC105370372
    nsv7075459inversion1nstd229human GRCh38 chr13: 110,952,781-112,398,036 , GRCh37.p13 chr13: 111,605,128-112,978,183 LOC102724489, LINC01044, 28 more genes
    nsv7074580inversion1nstd229human GRCh38 chr13: 110,243,158-113,630,621 , GRCh37.p13 chr13: 110,895,505-114,284,936 LINC01070, NAXD, 71 more genes
    nsv7058920inversion1nstd229human GRCh38 chr13: 112,379,157-112,386,225 , GRCh37.p13 chr13: 113,033,471-113,040,539 SPACA7, LOC105370372
    nsv6957758copy number variation1nstd229human GRCh38 chr13: 112,380,301-112,389,200 , GRCh37.p13 chr13: 113,034,615-113,043,514 SPACA7, LOC105370372
    nsv6956067copy number variation1nstd229human GRCh38 chr13: 112,401,221-112,401,257 , GRCh37.p13 chr13: 113,055,535-113,055,571 LOC105370372, SPACA7
    nsv6952148copy number variation1nstd229human GRCh38 chr13: 112,426,915-112,461,247 , GRCh37.p13 chr13: 113,081,229-113,115,561 SPACA7, LOC105370372
    nsv6946049copy number variation1nstd229human GRCh38 chr13: 112,349,406-112,385,732 , GRCh37.p13 chr13: 113,003,720-113,040,046 LOC105370372, SPACA7, 1 more genes
    nsv6944575copy number variation1nstd229human GRCh38 chr13: 112,422,013-112,433,867 , GRCh37.p13 chr13: 113,076,327-113,088,181 SPACA7, LOC105370372
    nsv6943460copy number variation1nstd229human GRCh38 chr13: 112,423,942-112,694,470 , GRCh37.p13 chr13: 113,160,258-113,348,784 ATP11A, TUBGCP3, 4 more genes
    nsv6943198copy number variation1nstd229human GRCh38 chr13: 111,028,013-113,621,089 , GRCh37.p13 chr13: 111,680,360-114,275,404 ARHGEF7, GRTP1, 52 more genes
    nsv6941505copy number variation1nstd229human GRCh38 chr13: 112,201,467-113,416,598 , GRCh37.p13 chr13: 112,924,380-114,070,913 LOC105370372, PCID2, 27 more genes
    nsv6940205copy number variation1nstd229human GRCh38 chr13: 112,399,419-112,405,550 , GRCh37.p13 chr13: 113,053,733-113,059,864 LOC105370372, SPACA7
    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
    nsv6637513copy number variation1nstd102humanUncertain significance GRCh37 chr13: 112,704,120-113,035,378 , GRCh38.p12 chr13|NT_187592.1: 1-182,034 , GRCh38.p12 chr13: 112,049,806-112,323,869 LOC105370372, LINC01043, 10 more genes
    nsv6637400copy number variation1nstd102humanPathogenic GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258 LOC107984609, LINC00354, 265 more genes
    nsv6637217copy number variation1nstd102humanPathogenic GRCh37 chr13: 99,421,603-115,107,733 , GRCh38.p12 chr13: 98,769,349-114,342,258 LOC107984609, CLYBL-AS2, 231 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6621645copy number variation1nstd224human GRCh37 chr13: 110,236,646-115,091,330 , GRCh38.p12 chr13: 109,584,299-114,325,855 PARP1P1, F7, 103 more genes
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