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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
    nsv7148025insertion1nstd232human GRCh37.p13 chr13: 113,909,441-113,909,441 , GRCh38.p12 chr13: 113,255,127-113,255,127 CUL4A
    nsv7074580inversion1nstd229human GRCh38 chr13: 110,243,158-113,630,621 , GRCh37.p13 chr13: 110,895,505-114,284,936 LINC01070, NAXD, 71 more genes
    nsv7070815inversion1nstd229human GRCh38 chr13: 113,138,744-113,361,865 , GRCh37.p13 chr13: 113,793,058-114,016,180 LDHBP1, GRTP1-AS1, 8 more genes
    nsv7068975inversion1nstd229human GRCh38 chr13: 113,202,910-113,389,554 , GRCh37.p13 chr13: 113,857,224-114,043,869 CUL4A, MIR8075, 5 more genes
    nsv6957635copy number variation1nstd229human GRCh38 chr13: 112,998,481-113,220,467 , GRCh37.p13 chr13: 113,652,795-113,874,781 KARS1P2, F7, 8 more genes
    nsv6954291copy number variation1nstd229human GRCh38 chr13: 113,188,524-113,224,939 , GRCh37.p13 chr13: 113,842,838-113,879,253 CUL4A, PCID2
    nsv6953414copy number variation1nstd229human GRCh38 chr13: 113,220,810-113,224,728 , GRCh37.p13 chr13: 113,875,124-113,879,042 CUL4A
    nsv6950892copy number variation1nstd229human GRCh38 chr13: 112,867,187-113,261,178 , GRCh37.p13 chr13: 113,521,501-113,915,492 KARS1P2, MCF2L-AS1, 11 more genes
    nsv6950327copy number variation1nstd229human GRCh38 chr13: 113,215,050-113,215,249 , GRCh37.p13 chr13: 113,869,364-113,869,563 CUL4A
    nsv6945720copy number variation1nstd229human GRCh38 chr13: 113,202,931-113,364,766 , GRCh37.p13 chr13: 113,857,245-114,019,081 CUL4A, MIR8075, 5 more genes
    nsv6943842copy number variation1nstd229human GRCh38 chr13: 113,208,234-113,208,258 , GRCh37.p13 chr13: 113,862,548-113,862,572 CUL4A, PCID2
    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
    nsv6942061copy number variation1nstd229human GRCh38 chr13: 113,115,566-113,228,529 , GRCh37.p13 chr13: 113,769,880-113,882,843 F10, LOC102724474, 6 more genes
    nsv6941505copy number variation1nstd229human GRCh38 chr13: 112,201,467-113,416,598 , GRCh37.p13 chr13: 112,924,380-114,070,913 LOC105370372, PCID2, 27 more genes
    nsv6941001copy number variation1nstd229human GRCh38 chr13: 113,223,071-113,223,344 , GRCh37.p13 chr13: 113,877,385-113,877,658 CUL4A
    nsv6939772copy number variation1nstd229human GRCh38 chr13: 113,165,787-113,258,280 , GRCh37.p13 chr13: 113,820,101-113,912,594 PCID2, CUL4A, 1 more genes
    nsv6938688copy number variation1nstd229human GRCh38 chr13: 113,204,822-113,208,144 , GRCh37.p13 chr13: 113,859,136-113,862,458 PCID2, CUL4A
    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
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