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Items: 1 to 20 of 234

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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
    nsv5901962copy number variation1nstd209human GRCh38 chr5: 38,865,797-38,866,438 , GRCh37.p13 chr5: 38,865,899-38,866,540 OSMR
    nsv5895594copy number variation1nstd209human GRCh38 chr5: 38,895,984-38,896,985 , GRCh37.p13 chr5: 38,896,086-38,897,087 OSMR
    nsv5895443copy number variation1nstd209human GRCh38 chr5: 38,928,129-38,928,182 , GRCh37.p13 chr5: 38,928,231-38,928,284 OSMR
    nsv5893853copy number variation1nstd209human GRCh38 chr5: 38,879,445-38,879,518 , GRCh37.p13 chr5: 38,879,547-38,879,620 OSMR
    nsv5842717copy number variation2nstd209human GRCh38 chr5: 38,895,916-38,897,015 , GRCh37.p13 chr5: 38,896,018-38,897,117 OSMR
    nsv5719894mobile element insertion1nstd211human GRCh38 chr5: 38,937,691-38,937,691 , GRCh37.p13 chr5: 38,937,793-38,937,793 RICTOR, OSMR
    nsv5715757mobile element insertion1nstd211human GRCh38 chr5: 38,937,679-38,937,679 , GRCh37.p13 chr5: 38,937,781-38,937,781 OSMR, RICTOR
    nsv5638438insertion1nstd207human GRCh38 chr5: 38,862,149-38,862,149 , GRCh37.p13 chr5: 38,862,251-38,862,251 OSMR
    nsv5634519insertion1nstd207human GRCh38 chr5: 38,862,297-38,862,297 , GRCh37.p13 chr5: 38,862,399-38,862,399 OSMR
    nsv5576353copy number variation1nstd207human GRCh38 chr5: 38,861,981-38,862,106 , GRCh37.p13 chr5: 38,862,083-38,862,208 OSMR
    nsv5572480copy number variation1nstd207human GRCh38 chr5: 38,928,129-38,928,182 , GRCh37.p13 chr5: 38,928,231-38,928,284 OSMR
    nsv5567288copy number variation1nstd207human GRCh38 chr5: 38,867,809-38,867,885 , GRCh37.p13 chr5: 38,867,911-38,867,987 OSMR
    nsv5560104mobile element insertion1nstd206human GRCh38 chr5: 38,937,692-38,937,742 , GRCh37.p13 chr5: 38,937,794-38,937,844 RICTOR, OSMR
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5458301copy number variation1nstd206human GRCh38 chr5: 38,926,088-38,926,146 , GRCh37.p13 chr5: 38,926,190-38,926,248 OSMR
    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
    nsv5368182translocation1nstd200human GRCh38 chr5: 38,879,519-38,879,519 , GRCh38 chr5: 38,879,446-38,879,446 , GRCh37.p13 chr5: 38,879,548-38,879,548 , GRCh37.p13 chr5: 38,879,621-38,879,621 OSMR
    nsv5368181translocation1nstd200human GRCh38 chr5: 38,857,629-38,857,629 , GRCh38 chr5: 38,854,954-38,854,954 , GRCh37.p13 chr5: 38,855,056-38,855,056 , GRCh37.p13 chr5: 38,857,731-38,857,731 OSMR
    nsv5344571translocation1nstd200human GRCh37 chr5: 38,855,056-38,855,056 , GRCh37 chr5: 38,857,731-38,857,731 , GRCh38.p12 chr5: 38,857,629-38,857,629 , GRCh38.p12 chr5: 38,854,954-38,854,954 OSMR
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