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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
    nsv7147445copy number variation1nstd232human GRCh37.p13 chr13: 113,763,066-113,763,184 , GRCh38.p12 chr13: 113,108,752-113,108,870 F7
    nsv7074580inversion1nstd229human GRCh38 chr13: 110,243,158-113,630,621 , GRCh37.p13 chr13: 110,895,505-114,284,936 LINC01070, NAXD, 71 more genes
    nsv6957636copy number variation1nstd229human GRCh38 chr13: 113,007,569-113,198,592 , GRCh37.p13 chr13: 113,661,883-113,852,906 F10, PROZ, 7 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
    nsv6956445copy number variation1nstd229human GRCh38 chr13: 113,104,137-113,120,625 , GRCh37.p13 chr13: 113,758,451-113,774,939 F7
    nsv6954554copy number variation1nstd229human GRCh38 chr13: 112,937,423-113,172,600 , GRCh37.p13 chr13: 113,591,737-113,826,914 PCID2, F10, 8 more genes
    nsv6953068copy number variation1nstd229human GRCh38 chr13: 112,957,374-113,115,914 , GRCh37.p13 chr13: 113,611,688-113,770,228 LOC107984591, F7, 2 more genes
    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
    nsv6944551copy number variation1nstd229human GRCh38 chr13: 113,090,601-113,104,200 , GRCh37.p13 chr13: 113,744,915-113,758,514 MCF2L, F7
    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
    nsv6940472copy number variation1nstd229human GRCh38 chr13: 112,439,101-113,131,800 , GRCh37.p13 chr13: 113,160,258-113,786,114 ATP11AUN, F10-AS1, 11 more genes
    nsv6939473copy number variation1nstd229human GRCh38 chr13: 113,112,472-113,113,218 , GRCh37.p13 chr13: 113,766,786-113,767,532 F7
    nsv6939096copy number variation1nstd229human GRCh38 chr13: 113,105,770-113,147,336 , GRCh37.p13 chr13: 113,760,084-113,801,650 F10, F10-AS1, 2 more genes
    nsv6938757copy number variation1nstd229human GRCh38 chr13: 113,042,230-113,204,304 , GRCh37.p13 chr13: 113,696,544-113,858,618 PROZ, KARS1P2, 6 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
    nsv6637559copy number variation1nstd102humanUncertain significance GRCh37 chr13: 113,196,617-113,800,575 , GRCh38.p12 chr13: 112,542,303-113,146,261 ATP11AUN, F10-AS1, 10 more genes
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