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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5500511copy number variation1nstd206human GRCh38 chr13: 50,099,962-50,100,402 , GRCh37.p13 chr13: 50,674,098-50,674,538 DLEU2, RPL18P10, 1 more genes
    nsv5307050copy number variation1nstd204human GRCh38.p13 chr13: 49,201,982-51,085,310 , GRCh37.p13 chr13: 49,776,118-51,659,446 , MLNR, 40 more genes
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4845274copy number variation1nstd200human GRCh37 chr13: 49,776,128-51,659,444 , GRCh38.p12 chr13: 49,201,992-51,085,308 , PHF11, 40 more genes
    nsv4728809copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 45,487,628-52,639,336 , GRCh38.p12 chr13: 44,913,493-52,065,200 ATP7B, RCBTB2, 155 more genes
    nsv4678858copy number variation1nstd189human GRCh37.p13 chr13: 50,484,195-51,548,156 , GRCh38.p12 chr13: 49,910,059-50,974,020 , DLEU2, 17 more genes
    nsv4604564copy number variation1nstd183human GRCh37 chr13: 50,587,410-51,453,495 , GRCh38.p12 chr13: 50,013,274-50,879,359 , RPL34P26, 13 more genes
    nsv4456820copy number variation1nstd102humanUncertain significance GRCh37 chr13: 49,586,017-61,311,845 , GRCh38.p12 chr13: 49,011,881-60,737,711 MIR759, CAB39L, 149 more genes
    nsv4425547copy number variation1nstd174human GRCh37 chr13: 50,513,535-51,404,018 , GRCh38.p12 chr13: 49,939,399-50,829,882 , KCNRG, 14 more genes
    nsv4381419copy number variation1nstd173human GRCh37 chr13: 46,589,256-51,939,619 , GRCh38.p12 chr13: 46,015,121-51,365,483 , RNU6-68P, 105 more genes
    nsv4217907copy number variation1nstd166human GRCh37.p13 chr13: 50,567,002-51,538,041 , GRCh38.p12 chr13: 49,992,866-50,963,905 , MIR15A, 16 more genes
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 LOC105370271, OR7E33P, 925 more genes
    nsv3924052copy number variation1nstd102humanPathogenic GRCh38 chr13: 41,288,493-85,137,552 , NCBI36 chr13: 40,760,629-84,609,688 , GRCh37 chr13: 41,862,629-85,711,687 TMEM272, LOC105370241, 535 more genes
    nsv3923911copy number variation1nstd102humanPathogenic GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921 MLNR, SIAH3, 422 more genes
    nsv3923642copy number variation1nstd102humanPathogenic GRCh37 chr13: 44,738,887-115,085,141 , NCBI36 chr13: 43,636,887-114,110,750 , GRCh38 chr13: 44,164,751-114,327,173 LOC107984554, HNRNPA1P18, 861 more genes
    nsv3923636copy number variation1nstd102humanPathogenic NCBI36 chr13: 37,986,314-50,897,351 , GRCh37 chr13: 39,088,314-51,999,350 , GRCh38 chr13: 38,514,177-51,425,214 TUSC8, SNORA31B, 251 more genes
    nsv3922463copy number variation1nstd102humanPathogenic NCBI36 chr13: 18,418,322-114,088,205 , GRCh37 chr13: 19,520,322-115,070,103 , GRCh38 chr13: 18,946,182-114,304,628 TULP3P1, LOC105370349, 1311 more genes
    nsv3921223copy number variation1nstd102humanPathogenic GRCh38 chr13: 19,671,934-114,340,331 , NCBI36 chr13: 19,144,074-114,123,908 , GRCh37 chr13: 20,246,074-115,085,141 TRIM60P13, LINC00351, 1289 more genes
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