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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5898593copy number variation1nstd209human GRCh38 chr5: 40,779,155-40,786,710 , GRCh37.p13 chr5: 40,779,257-40,786,812 PRKAA1
    nsv5898063copy number variation1nstd209human GRCh38 chr5: 40,794,513-40,794,873 , GRCh37.p13 chr5: 40,794,615-40,794,975 PRKAA1
    nsv5887603copy number variation1nstd209human GRCh38 chr5: 40,768,082-40,768,204 , GRCh37.p13 chr5: 40,768,184-40,768,306 PRKAA1
    nsv5842981copy number variation1nstd209human GRCh38 chr5: 40,779,092-40,786,714 , GRCh37.p13 chr5: 40,779,194-40,786,816 PRKAA1
    nsv5691116mobile element insertion1nstd211human GRCh38 chr5: 40,769,116-40,769,116 , GRCh37.p13 chr5: 40,769,218-40,769,218 PRKAA1
    nsv5627906insertion1nstd207human GRCh38 chr5: 40,768,082-40,768,082 , GRCh37.p13 chr5: 40,768,184-40,768,184 PRKAA1
    nsv5575267copy number variation1nstd207human GRCh38 chr5: 40,794,513-40,794,873 , GRCh37.p13 chr5: 40,794,615-40,794,975 PRKAA1
    nsv5472347copy number variation1nstd206human GRCh38 chr5: 40,786,663-40,787,371 , GRCh37.p13 chr5: 40,786,765-40,787,473 PRKAA1
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5468478copy number variation1nstd206human GRCh38 chr5: 40,771,353-40,781,305 , GRCh37.p13 chr5: 40,771,455-40,781,407 PRKAA1
    nsv5466540copy number variation1nstd206human GRCh38 chr5: 40,794,513-40,794,876 , GRCh37.p13 chr5: 40,794,615-40,794,978 PRKAA1
    nsv5457177copy number variation1nstd206human GRCh38 chr5: 40,779,155-40,786,719 , GRCh37.p13 chr5: 40,779,257-40,786,821 PRKAA1
    nsv5456315copy number variation1nstd206human GRCh38 chr5: 40,768,082-40,768,206 , GRCh37.p13 chr5: 40,768,184-40,768,308 PRKAA1
    nsv5395690mobile element insertion1nstd206human GRCh38 chr5: 40,769,116-40,769,167 , GRCh37.p13 chr5: 40,769,218-40,769,269 PRKAA1
    nsv5387272copy number variation1nstd186human GRCh37 chr5: 40,794,884-40,794,978 , GRCh38.p12 chr5: 40,794,782-40,794,876 PRKAA1
    nsv5386960copy number variation1nstd186human GRCh37 chr5: 40,794,614-40,794,674 , GRCh38.p12 chr5: 40,794,512-40,794,572 PRKAA1
    nsv5386489copy number variation3nstd186human GRCh37 chr5: 40,794,615-40,794,978 , GRCh38.p12 chr5: 40,794,513-40,794,876 PRKAA1
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5312288copy number variation1nstd204human GRCh38.p13 chr5: 40,794,513-40,794,876 , GRCh37.p13 chr5: 40,794,615-40,794,978 PRKAA1
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