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Items: 1 to 20 of 325

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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
    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
    nsv6955496copy number variation1nstd229human GRCh38 chr13: 106,510,610-106,510,717 , GRCh37.p13 chr13: 107,162,958-107,163,065 EFNB2
    nsv6955288copy number variation1nstd229human GRCh38 chr13: 106,045,375-107,281,617 , GRCh37.p13 chr13: 106,697,724-107,933,965 LINC00443, NALF1, 13 more genes
    nsv6949196copy number variation1nstd229human GRCh38 chr13: 106,510,590-106,510,776 , GRCh37.p13 chr13: 107,162,938-107,163,124 EFNB2
    nsv6943480copy number variation1nstd229human GRCh38 chr13: 106,500,094-106,500,290 , GRCh37.p13 chr13: 107,152,442-107,152,638 EFNB2
    nsv6943163copy number variation1nstd229human GRCh38 chr13: 106,520,996-106,521,122 , GRCh37.p13 chr13: 107,173,344-107,173,470 EFNB2
    nsv6942577copy number variation1nstd229human GRCh38 chr13: 106,497,054-106,497,412 , GRCh37.p13 chr13: 107,149,402-107,149,760 EFNB2
    nsv6938831copy number variation1nstd229human GRCh38 chr13: 106,527,103-106,531,679 , GRCh37.p13 chr13: 107,179,451-107,184,027 EFNB2
    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
    nsv6637531copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,334,135-110,383,902 , GRCh38.p12 chr13: 99,681,881-109,731,555 ARGLU1, LINC00343, 101 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
    nsv6621642copy number variation1nstd224human GRCh37 chr13: 106,517,830-107,646,908 , GRCh38.p12 chr13: 105,865,481-106,994,560 LINC00460, ATP5MC1P5, 12 more genes
    nsv6594777inversion1nstd223human GRCh38 chr13: 104,930,881-106,737,596 , GRCh37.p13 chr13: 105,583,232-107,389,944 LINC00460, DAOA-AS1, 16 more genes
    nsv6492108copy number variation1nstd223human GRCh38 chr13: 106,510,589-106,510,776 , GRCh37.p13 chr13: 107,162,937-107,163,124 EFNB2
    nsv6479713copy number variation1nstd223human GRCh38 chr13: 106,532,801-106,536,900 , GRCh37.p13 chr13: 107,185,149-107,189,248 EFNB2
    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
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