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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
    nsv7138101insertion1nstd232human GRCh37.p13 chr5: 5,132,429-5,132,429 , GRCh38.p12 chr5: 5,132,316-5,132,316 ADAMTS16-DT
    nsv7053901inversion1nstd229human GRCh38 chr5: 3,129,013-8,027,353 , GRCh37.p13 chr5: 3,129,127-8,027,466 FASTKD3, LOC101929200, 58 more genes
    nsv7045426inversion1nstd229human GRCh38 chr5: 3,060,043-5,252,130 , GRCh37.p13 chr5: 3,060,157-5,252,243 LOC107986400, LINC02063, 16 more genes
    nsv7045223inversion1nstd229human GRCh38 chr5: 2,721,510-7,652,208 , GRCh37.p13 chr5: 2,721,624-7,652,321 LOC105374620, LOC105374634, 60 more genes
    nsv7042270inversion1nstd229human GRCh38 chr5: 4,344,295-6,275,858 , GRCh37.p13 chr5: 4,344,408-6,275,971 LOC105374629, MTCO2P30, 15 more genes
    nsv7040546inversion1nstd229human GRCh38 chr5: 4,326,347-6,141,150 , GRCh37.p13 chr5: 4,326,460-6,141,263 LOC105374634, MTCO1P31, 15 more genes
    nsv6774652copy number variation1nstd229human GRCh38 chr5: 4,946,640-6,484,597 , GRCh37.p13 chr5: 4,946,753-6,484,710 RN7SKP73, LINC01020, 17 more genes
    nsv6768166copy number variation1nstd229human GRCh38 chr5: 5,119,859-5,130,907 , GRCh37.p13 chr5: 5,119,972-5,131,020 ADAMTS16-DT, RN7SKP73
    nsv6765199copy number variation1nstd229human GRCh38 chr5: 5,093,729-5,718,574 , GRCh37.p13 chr5: 5,093,842-5,718,687 MTCO1P30, ADAMTS16, 8 more genes
    nsv6761354copy number variation1nstd229human GRCh38 chr5: 4,162,209-5,312,683 , GRCh37.p13 chr5: 4,162,322-5,312,796 ADAMTS16-DT, LINC02114, 8 more genes
    nsv6758455copy number variation1nstd229human GRCh38 chr5: 4,821,867-5,407,686 , GRCh37.p13 chr5: 4,821,980-5,407,799 ADAMTS16, LOC101929200, 11 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
    nsv6574354inversion1nstd223human GRCh38 chr5: 2,721,509-7,652,209 , GRCh37.p13 chr5: 2,721,623-7,652,322 MIR4278, LOC442132, 60 more genes
    nsv6387172copy number variation1nstd223human GRCh38 chr5: 4,921,419-5,324,443 , GRCh37.p13 chr5: 4,921,532-5,324,556 ADAMTS16-DT, ADAMTS16, 5 more genes
    nsv6378923copy number variation1nstd223human GRCh38 chr5: 4,162,209-5,312,683 , GRCh37.p13 chr5: 4,162,322-5,312,796 RN7SKP73, LINC01020, 8 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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