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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
    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
    nsv7060236inversion1nstd229human GRCh38 chr13: 109,400,177-111,221,158 , GRCh37.p13 chr13: 110,052,524-111,873,505 LINC00399, ANKRD10, 36 more genes
    nsv6956641copy number variation1nstd229human GRCh38 chr13: 111,075,901-111,273,900 , GRCh37.p13 chr13: 111,728,248-111,926,247 ARHGEF7, ARHGEF7-AS2, 4 more genes
    nsv6954592copy number variation1nstd229human GRCh38 chr13: 110,322,299-111,271,113 , GRCh37.p13 chr13: 110,974,646-111,923,460 ARHGEF7-AS2, LINC00567, 22 more genes
    nsv6949431copy number variation1nstd229human GRCh38 chr13: 111,148,161-111,148,369 , GRCh37.p13 chr13: 111,800,508-111,800,716 LOC101060553, ARHGEF7, 1 more genes
    nsv6949226copy number variation1nstd229human GRCh38 chr13: 110,979,901-111,157,400 , GRCh37.p13 chr13: 111,632,248-111,809,747 LINC00431, ARHGEF7, 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
    nsv6941729copy number variation1nstd229human GRCh38 chr13: 111,148,484-111,150,643 , GRCh37.p13 chr13: 111,800,831-111,802,990 LOC101060553, ARHGEF7-AS1, 1 more genes
    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
    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
    nsv6315552copy number variation1nstd102humanPathogenic GRCh37 chr13: 89,490,345-115,062,235 , GRCh38.p12 chr13: 88,838,091-114,296,760 MIR20A, MIR548AR, 347 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6315465copy number variation1nstd102humanPathogenic GRCh37 chr13: 110,428,062-115,107,733 , GRCh38.p12 chr13: 109,775,715-114,342,258 SALL4P4, KARS1P2, 103 more genes
    nsv6314171copy number variation1nstd102humanPathogenic GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258 MIR4705, LOC102724149, 430 more genes
    nsv6314066copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,258,328-115,107,733 , GRCh38.p12 chr13: 99,606,074-114,342,258 MIR4502, GRTP1-AS1, 208 more genes
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