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Items: 1 to 20 of 463

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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
    nsv7074580inversion1nstd229human GRCh38 chr13: 110,243,158-113,630,621 , GRCh37.p13 chr13: 110,895,505-114,284,936 LINC01070, NAXD, 71 more genes
    nsv7066153inversion1nstd229human GRCh38 chr13: 113,377,803-114,332,425 , GRCh37.p13 chr13: 114,032,118-115,085,141 TMCO3, GRK1, 26 more genes
    nsv6952867copy number variation1nstd229human GRCh38 chr13: 113,596,610-113,603,332 , GRCh37.p13 chr13: 114,250,925-114,257,647 TFDP1
    nsv6952106copy number variation1nstd229human GRCh38 chr13: 113,350,847-113,586,194 , GRCh37.p13 chr13: 114,005,162-114,240,509 GRTP1, TFDP1, 5 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
    nsv6942847copy number variation1nstd229human GRCh38 chr13: 113,098,406-113,791,902 , GRCh37.p13 chr13: 113,752,720-114,494,875 MIR8075, ATP4B, 22 more genes
    nsv6940449copy number variation1nstd229human GRCh38 chr13: 113,600,785-113,600,857 , GRCh37.p13 chr13: 114,255,100-114,255,172 TFDP1
    nsv6939406copy number variation1nstd229human GRCh38 chr13: 113,617,461-113,789,008 , GRCh37.p13 chr13: 114,271,776-114,491,981 TFDP1, LINC00552, 4 more genes
    nsv6939090copy number variation1nstd229human GRCh38 chr13: 113,366,353-113,584,698 , GRCh37.p13 chr13: 114,020,668-114,239,013 ADPRHL1, TFDP1, 3 more genes
    nsv6938484copy number variation1nstd229human GRCh38 chr13: 113,562,955-114,319,153 , GRCh37.p13 chr13: 114,217,270-115,084,628 CDC16, TMEM255B, 21 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
    nsv6493301copy number variation1nstd223human GRCh38 chr13: 113,593,330-113,594,467 , GRCh37.p13 chr13: 114,247,645-114,248,782 TFDP1
    nsv6489466copy number variation1nstd223human GRCh38 chr13: 113,625,611-113,626,134 , GRCh37.p13 chr13: 114,279,926-114,280,449 TFDP1
    nsv6480967copy number variation1nstd223human GRCh38 chr13: 113,350,847-113,586,198 , GRCh37.p13 chr13: 114,005,162-114,240,513 DCUN1D2, GRTP1, 5 more genes
    nsv6480792copy number variation1nstd223human GRCh38 chr13: 113,593,642-113,594,601 , GRCh37.p13 chr13: 114,247,957-114,248,916 TFDP1
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