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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
    nsv7052860inversion1nstd229human GRCh38 chr5: 10,170,489-10,504,221 , GRCh37.p13 chr5: 10,170,601-10,504,333 CMBL, MIR10397, 11 more genes
    nsv7038962inversion1nstd229human GRCh38 chr5: 10,348,795-10,536,524 , GRCh37.p13 chr5: 10,348,907-10,536,636 RPL30P7, ROPN1L-AS1, 7 more genes
    nsv6770909copy number variation1nstd229human GRCh38 chr5: 10,501,941-10,509,195 , GRCh37.p13 chr5: 10,502,053-10,509,307 LINC02213, LINC02212
    nsv6768721copy number variation1nstd229human GRCh38 chr5: 10,521,711-10,521,760 , GRCh37.p13 chr5: 10,521,823-10,521,872 LINC02213
    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
    nsv6765155copy number variation1nstd229human GRCh38 chr5: 10,514,804-10,520,148 , GRCh37.p13 chr5: 10,514,916-10,520,260 LINC02213
    nsv6764233copy number variation1nstd229human GRCh38 chr5: 10,518,000-10,521,124 , GRCh37.p13 chr5: 10,518,112-10,521,236 LINC02213
    nsv6762884copy number variation1nstd229human GRCh38 chr5: 10,508,763-10,508,808 , GRCh37.p13 chr5: 10,508,875-10,508,920 LINC02213
    nsv6760426copy number variation1nstd229human GRCh38 chr5: 10,502,132-10,505,705 , GRCh37.p13 chr5: 10,502,244-10,505,817 LINC02213, LINC02212
    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
    nsv6572907inversion1nstd223human GRCh38 chr5: 10,505,780-10,507,279 , GRCh37.p13 chr5: 10,505,892-10,507,391 LINC02213
    nsv6557422inversion1nstd223human GRCh38 chr5: 10,505,844-10,507,183 , GRCh37.p13 chr5: 10,505,956-10,507,295 LINC02213
    nsv6389181copy number variation1nstd223human GRCh38 chr5: 10,429,509-10,543,017 , GRCh37.p13 chr5: 10,429,621-10,543,129 MARCHF6, ROPN1L, 5 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
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