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Items: 1 to 20 of 312

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887963copy number variation1nstd209human GRCh38 chr5: 55,329,778-55,330,600 , GRCh37.p13 chr5: 54,625,606-54,626,428 MTREX
    nsv5724041mobile element insertion1nstd211human GRCh38 chr5: 55,330,398-55,330,398 , GRCh37.p13 chr5: 54,626,226-54,626,226 MTREX
    nsv5565326copy number variation1nstd207human GRCh38 chr5: 55,329,778-55,330,600 , GRCh37.p13 chr5: 54,625,606-54,626,428 MTREX
    nsv5556704mobile element insertion1nstd206human GRCh38 chr5: 55,330,398-55,330,449 , GRCh37.p13 chr5: 54,626,226-54,626,277 MTREX
    nsv5472742copy number variation1nstd206human GRCh38 chr5: 55,330,536-55,334,978 , GRCh37.p13 chr5: 54,626,364-54,630,806 MTREX
    nsv5470355copy number variation1nstd206human GRCh38 chr5: 55,314,893-55,314,960 , GRCh37.p13 chr5: 54,610,721-54,610,788 MTREX
    nsv5455610copy number variation1nstd206human GRCh38 chr5: 55,329,780-55,330,601 , GRCh37.p13 chr5: 54,625,608-54,626,429 MTREX
    nsv5368405translocation1nstd200human GRCh38 chr9: 120,152,084-120,152,084 , GRCh38 chr5: 55,316,875-55,316,875 , GRCh37.p13 chr5: 54,612,703-54,612,703 , GRCh37.p13 chr9: 122,914,362-122,914,362 MTREX
    nsv5368402translocation1nstd200human GRCh38 chr5: 55,228,540-55,228,540 , GRCh38 chr5: 55,338,906-55,338,906 , GRCh37.p13 chr5: 54,634,734-54,634,734 , GRCh37.p13 chr5: 54,524,368-54,524,368 MTREX
    nsv5335292translocation1nstd200human GRCh37 chr5: 54,524,368-54,524,368 , GRCh37 chr5: 54,634,734-54,634,734 , GRCh38.p12 chr5: 55,338,906-55,338,906 , GRCh38.p12 chr5: 55,228,540-55,228,540 MTREX
    nsv5331461translocation1nstd200human GRCh37 chr5: 54,604,323-54,604,323 , GRCh37 chr5: 54,604,382-54,604,382 , GRCh38.p12 chr5: 55,308,495-55,308,495 , GRCh38.p12 chr5: 55,308,554-55,308,554 MTREX
    nsv5318485copy number variation1nstd204human GRCh38.p13 chr5: 55,329,756-55,330,623 , GRCh37.p13 chr5: 54,625,584-54,626,451 MTREX
    nsv5099403mobile element insertion1nstd203human GRCh38 chr5: 55,340,883-55,340,897 , GRCh37.p13 chr5: 54,636,711-54,636,725 MTREX
    nsv5095412mobile element insertion1nstd203human GRCh38 chr5: 55,359,238-55,359,251 , GRCh37.p13 chr5: 54,655,066-54,655,079 MTREX
    nsv5094702mobile element insertion1nstd203human GRCh38 chr5: 55,362,098-55,362,105 , GRCh37.p13 chr5: 54,657,926-54,657,933 MTREX
    nsv5091513mobile element insertion1nstd203human GRCh38 chr5: 55,352,306-55,352,306 , GRCh37.p13 chr5: 54,648,134-54,648,134 MTREX
    nsv5085516mobile element insertion1nstd203human GRCh38 chr5: 55,378,363-55,378,382 , GRCh37.p13 chr5: 54,674,191-54,674,210 MTREX, LOC107986415
    nsv4944914copy number variation1nstd200human GRCh38 chr5: 55,355,710-55,887,901 , GRCh37.p13 chr5: 54,651,538-55,183,729 , MIR5687, 12 more genes
    nsv4931589copy number variation1nstd200human GRCh38 chr5: 55,390,753-55,390,824 , GRCh37.p13 chr5: 54,686,581-54,686,652 MTREX
    nsv4931588copy number variation1nstd200human GRCh38 chr5: 55,389,126-55,389,203 , GRCh37.p13 chr5: 54,684,954-54,685,031 MTREX
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