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Items: 1 to 20 of 293

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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
    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
    nsv7064561inversion1nstd229human GRCh38 chr13: 110,860,798-111,025,886 , GRCh37.p13 chr13: 111,513,145-111,678,233 PARP1P1, ANKRD10, 3 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
    nsv7060211inversion1nstd229human GRCh38 chr13: 110,858,984-111,100,986 , GRCh37.p13 chr13: 111,511,331-111,753,333 ANKRD10, PRECSIT, 4 more genes
    nsv7059605inversion1nstd229human GRCh38 chr13: 110,238,294-111,024,734 , GRCh37.p13 chr13: 110,890,641-111,677,081 COL4A1, RPL21P107, 17 more genes
    nsv6957649copy number variation1nstd229human GRCh38 chr13: 110,973,155-111,020,015 , GRCh37.p13 chr13: 111,625,502-111,672,362 LOC105370364, LINC00431
    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
    nsv6953938copy number variation1nstd229human GRCh38 chr13: 110,971,893-110,972,084 , GRCh37.p13 chr13: 111,624,240-111,624,431 LINC00431, LOC105370364
    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
    nsv6947196copy number variation1nstd229human GRCh38 chr13: 110,942,300-110,991,590 , GRCh37.p13 chr13: 111,594,647-111,643,937 LOC105370364, LINC00431
    nsv6941965copy number variation1nstd229human GRCh38 chr13: 110,965,375-110,965,510 , GRCh37.p13 chr13: 111,617,722-111,617,857 LOC105370364, LINC00431
    nsv6941617copy number variation1nstd229human GRCh38 chr13: 110,982,801-110,988,100 , GRCh37.p13 chr13: 111,635,148-111,640,447 LINC00431
    nsv6941601copy number variation1nstd229human GRCh38 chr13: 110,975,844-110,978,587 , GRCh37.p13 chr13: 111,628,191-111,630,934 LINC00431
    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
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