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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7098841copy number variation1nstd102humanPathogenic GRCh37 chr5: 10,149,255-18,180,300 , GRCh38.p12 chr5: 10,149,143-18,180,191 RN7SKP133, TAF11L1, 102 more genes
    nsv6775248copy number variation1nstd229human GRCh38 chr5: 10,532,001-10,793,300 , GRCh37.p13 chr5: 10,532,113-10,793,412 DAP-DT, CTD-2154B17.1, 3 more genes
    nsv6766002copy number variation1nstd229human GRCh38 chr5: 10,203,601-10,797,600 , GRCh37.p13 chr5: 10,203,713-10,797,712 LOC645763, DAP, 16 more genes
    nsv6637149copy number variation1nstd102humanPathogenic GRCh37 chr5: 8,081,005-22,210,970 , GRCh38.p12 chr5: 8,080,892-22,210,861 LOC107986376, MARCHF11, 150 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636849copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-17,654,787 , GRCh38.p12 chr5: 113,462-17,654,678 ADCY2, HMGB3P3, 248 more genes
    nsv6636672copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743 LINC02123, LINC01020, 302 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 BASP1, RNU1-76P, 338 more genes
    nsv6630206copy number variation1nstd224human GRCh37 chr5: 10,578,303-11,233,371 , GRCh38.p12 chr5: 10,578,191-11,233,259 CTNND2, DAP, 6 more genes
    nsv6315441copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-29,310,520 , GRCh38.p12 chr5: 113,461-29,310,413 FBXL7, LOC105374608, 319 more genes
    nsv6315416copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269 LOC105374649, LINC02196, 333 more genes
    nsv6315334copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-12,601,027 , GRCh38.p12 chr5: 113,461-12,600,915 LOC105374642, LOC107986395, 173 more genes
    nsv6291096copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-16,952,167 , GRCh38.p12 chr5: 113,462-16,952,058 MIR4457, HNRNPKP5, 222 more genes
    nsv6136143copy number variation1nstd213human GRCh37 chr5: 9,360,000-26,560,001 , GRCh38.p12 chr5: 9,359,888-26,559,892 FTH1P10, MYO10, 163 more genes
    nsv6135687copy number variation1nstd213human GRCh37 chr5: 9,400,000-26,970,001 , GRCh38.p12 chr5: 9,399,888-26,969,894 DNAH5, MSNP1, 165 more genes
    nsv6135635copy number variation1nstd213human GRCh37 chr5: 10,090,000-11,250,001 , GRCh38.p12 chr5: 10,089,888-11,249,889 ROPN1L, CMBL, 19 more genes
    nsv6135433copy number variation1nstd213human GRCh37 chr5: 6,670,000-11,470,001 , GRCh38.p12 chr5: 6,669,887-11,469,889 CTNND2, TENT4A, 68 more genes
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv4794893copy number variation1nstd200human GRCh37 chr5: 10,520,576-10,991,032 , GRCh38.p12 chr5: 10,520,464-10,990,920 CTNND2, LINC02213, 6 more genes
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