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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3123997copy number variation2nstd151human GRCh37 chr1: 100,605,202-100,605,812 , GRCh38.p12 chr1: 100,139,646-100,140,256 TRMT13
    esv2997142copy number variation1estd209human GRCh37 chr1: 100,602,396-100,602,397 , GRCh38.p12 chr1: 100,136,840-100,136,841 TRMT13
    esv275107copy number variation1estd176human NCBI36 chr1: 100,374,353-100,377,901 , GRCh37.p13 chr1: 100,601,765-100,605,313 , GRCh38.p12 chr1: 100,136,209-100,139,757 TRMT13
    esv3383157copy number variation1estd59human NCBI36 chr1: 100,376,379-100,376,586 , GRCh37.p13 chr1: 100,603,791-100,603,998 , GRCh38.p12 chr1: 100,138,235-100,138,442 TRMT13
    nsv5410312mobile element insertion1nstd206human GRCh38 chr1: 100,143,954-100,144,005 , GRCh37.p13 chr1: 100,609,510-100,609,561 TRMT13
    nsv6256226mobile element insertion1nstd215human GRCh38 chr1: 100,143,954-100,143,954 , GRCh37.p13 chr1: 100,609,510-100,609,510 TRMT13
    nsv5690177mobile element insertion2nstd211human GRCh38 chr1: 100,143,954-100,143,954 , GRCh37.p13 chr1: 100,609,510-100,609,510 TRMT13
    nsv5613730insertion1nstd207human GRCh38 chr1: 100,143,944-100,143,944 , GRCh37.p13 chr1: 100,609,500-100,609,500 TRMT13
    nsv4537218insertion1nstd166human GRCh37.p13 chr1: 100,603,910-100,603,910 , GRCh38.p12 chr1: 100,138,354-100,138,354 TRMT13
    nsv4458552mobile element insertion1nstd166human GRCh37.p13 chr1: 100,609,500-100,609,500 , GRCh38.p12 chr1: 100,143,944-100,143,944 TRMT13
    nsv4458551mobile element insertion1nstd166human GRCh37.p13 chr1: 100,604,909-100,604,909 , GRCh38.p12 chr1: 100,139,353-100,139,353 TRMT13
    nsv3076212mobile element insertion1nstd144human GRCh37 chr1: 100,609,500-100,609,500 , GRCh38.p12 chr1: 100,143,944-100,143,944 TRMT13
    esv2189189insertion1estd194human NCBI36 chr1: 100,373,529-100,373,529 , GRCh37.p13 chr1: 100,600,941-100,600,941 , GRCh38.p12 chr1: 100,135,385-100,135,385 TRMT13
    nsv1454302short tandem repeat1nstd128human GRCh37 chr1: 100,609,231-100,609,255 , GRCh38.p12 chr1: 100,143,675-100,143,699 TRMT13
    nsv1452416short tandem repeat1nstd128human GRCh37 chr1: 100,604,513-100,604,533 , GRCh38.p12 chr1: 100,138,957-100,138,977 TRMT13
    nsv1452415short tandem repeat2nstd128human GRCh37 chr1: 100,599,626-100,599,641 , GRCh38.p12 chr1: 100,134,070-100,134,085 TRMT13
    nsv1498427short tandem repeat1nstd128human GRCh37 chr1: 100,602,919-100,602,933 , GRCh38.p12 chr1: 100,137,363-100,137,377 TRMT13
    nsv1454815short tandem repeat3nstd128human GRCh37 chr1: 100,610,124-100,610,135 , GRCh38.p12 chr1: 100,144,568-100,144,579 TRMT13
    nsv6638243copy number variation1nstd229human GRCh38 chr1: 100,148,498-100,161,772 , GRCh37.p13 chr1: 100,614,054-100,627,328 TRMT13, LRRC39
    nsv6638242copy number variation1nstd229human GRCh38 chr1: 100,145,020-100,149,723 , GRCh37.p13 chr1: 100,610,576-100,615,279 TRMT13, LRRC39
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