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Items: 1 to 20 of 268

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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
    nsv6957013copy number variation1nstd229human GRCh38 chr13: 112,067,264-112,068,043 , GRCh37.p13 chr13: 112,721,578-112,722,357 SOX1, SOX1-OT
    nsv6952895copy number variation1nstd229human GRCh38 chr13: 112,069,228-112,072,252 , GRCh37.p13 chr13: 112,723,542-112,726,566 SOX1, SOX1-OT
    nsv6947110copy number variation1nstd229human GRCh38 chr13: 112,049,201-112,079,200 , GRCh37.p13 chr13: 112,703,515-112,733,514 SOX1-OT, SOX1
    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
    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
    nsv6489591copy number variation1nstd223human GRCh38 chr13: 112,065,001-112,068,900 , GRCh37.p13 chr13: 112,719,315-112,723,214 SOX1, SOX1-OT
    nsv6485750copy number variation1nstd223human GRCh38 chr13: 112,067,501-112,070,600 , GRCh37.p13 chr13: 112,721,815-112,724,914 SOX1-OT, SOX1
    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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