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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112795copy number variation1nstd102humanPathogenic GRCh37 chr18: 64,996-6,838,315 , GRCh38.p12 chr18: 64,996-6,838,316 TYMSOS, LOC107985176, 104 more genes
    nsv5946416copy number variation1nstd209human GRCh38 chr18: 630,328-657,139 , GRCh37.p13 chr18: 630,328-657,139 TYMS, CLUL1, 2 more genes
    nsv5938104copy number variation1nstd209human GRCh38 chr18: 657,645-657,700 , GRCh37.p13 chr18: 657,645-657,700 TYMSOS, TYMS
    nsv5932383copy number variation1nstd209human GRCh38 chr18: 654,174-655,925 , GRCh37.p13 chr18: 654,174-655,925 TYMSOS, TYMS
    nsv5879337copy number variation1nstd209human GRCh38 chr18: 630,821-657,135 , GRCh37.p13 chr18: 630,821-657,135 TYMS, CLUL1, 2 more genes
    nsv5871283copy number variation1nstd209human GRCh38 chr18: 653,910-656,009 , GRCh37.p13 chr18: 653,910-656,009 TYMS, TYMSOS
    nsv5710903mobile element insertion1nstd211human GRCh38 chr18: 650,571-650,571 , GRCh37.p13 chr18: 650,571-650,571 CLUL1, TYMSOS
    nsv5531915copy number variation1nstd206human GRCh38 chr18: 651,314-654,346 , GRCh37.p13 chr18: 651,314-654,346 TYMSOS
    nsv5526225copy number variation1nstd206human GRCh38 chr18: 643,576-647,817 , GRCh37.p13 chr18: 643,576-647,817 TYMSOS, CLUL1
    nsv5522430copy number variation1nstd206human GRCh38 chr18: 654,174-655,930 , GRCh37.p13 chr18: 654,174-655,930 TYMSOS, TYMS
    nsv5520555copy number variation1nstd206human GRCh38 chr18: 559,000-844,000 , GRCh37.p13 chr18: 559,000-844,001 RNU1-109P, LOC105371952, 8 more genes
    nsv5514109copy number variation1nstd206human GRCh38 chr18: 350,000-744,000 , GRCh37.p13 chr18: 350,000-744,000 LOC107985155, LINC01925, 9 more genes
    nsv5415763mobile element insertion1nstd206human GRCh38 chr18: 650,571-650,622 , GRCh37.p13 chr18: 650,571-650,622 TYMSOS, CLUL1
    nsv5321993copy number variation1nstd204human GRCh37.p13 chr18: 654,167-655,932 , GRCh38.p13 chr18: 654,167-655,932 TYMS, TYMSOS
    nsv5294649copy number variation1nstd204human GRCh38.p13 chr18: 654,001-655,900 , GRCh37.p13 chr18: 654,001-655,900 TYMS, TYMSOS
    nsv5283473copy number variation1nstd204human GRCh38.p13 chr18: 654,210-655,909 , GRCh37.p13 chr18: 654,210-655,909 TYMS, TYMSOS
    nsv5017222copy number variation1nstd200human GRCh38 chr18: 654,174-655,930 , GRCh37.p13 chr18: 654,174-655,930 TYMS, TYMSOS
    nsv5017206copy number variation1nstd200human GRCh38 chr18: 368,766-722,966 , GRCh37.p13 chr18: 368,766-722,966 LOC105371952, RN7SKP146, 9 more genes
    nsv5014176copy number variation1nstd200human GRCh38 chr18: 483,198-725,642 , GRCh37.p13 chr18: 483,198-725,642 CLUL1, TYMSOS, 8 more genes
    nsv5014175copy number variation1nstd200human GRCh38 chr18: 465,329-684,322 , GRCh37.p13 chr18: 465,329-684,322 CETN1, CLUL1, 7 more genes
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