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Items: 1 to 20 of 928

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139328copy number variation1nstd232human GRCh37.p13 chr5: 79,987,767-79,987,838 , GRCh38.p12 chr5: 80,691,948-80,692,019 MSH3
    nsv7137224copy number variation1nstd232human GRCh37.p13 chr5: 80,169,103-80,169,160 , GRCh38.p12 chr5: 80,873,284-80,873,341 MSH3
    nsv7097548copy number variation1nstd102humanUncertain significance GRCh37 chr5: 80,057,355-80,109,570 , GRCh38.p12 chr5: 80,761,536-80,813,751 MSH3
    nsv7097547copy number variation1nstd102humanUncertain significance GRCh37 chr5: 80,037,273-80,040,444 , GRCh38.p12 chr5: 80,741,454-80,744,625 MSH3
    nsv7097546copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,949,868-80,088,673 , GRCh38.p12 chr5: 80,654,049-80,792,854 MSH3, DHFR
    nsv7097297copy number variation1nstd102humanUncertain significance GRCh37 chr5: 80,171,560-80,171,681 , GRCh38.p12 chr5: 80,875,741-80,875,862 MSH3
    nsv7097296copy number variation1nstd102humanUncertain significance GRCh37 chr5: 80,088,542-80,109,570 , GRCh38.p12 chr5: 80,792,723-80,813,751 MSH3
    nsv7097295copy number variation1nstd102humanPathogenic GRCh37 chr5: 80,063,742-80,071,587 , GRCh38.p12 chr5: 80,767,923-80,775,768 MSH3
    nsv7097294copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 80,024,660-80,024,794 , GRCh38.p12 chr5: 80,728,841-80,728,975 MSH3
    nsv7097293copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,924,906-80,171,681 , GRCh38.p12 chr5: 80,629,087-80,875,862 DHFR, MTRNR2L2, 2 more genes
    nsv7097162copy number variation1nstd102humanPathogenic GRCh37 chr5: 79,960,952-80,063,949 , GRCh38.p12 chr5: 80,665,133-80,768,130 MSH3
    nsv7097161copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,949,868-80,040,444 , GRCh38.p12 chr5: 80,654,049-80,744,625 MSH3, DHFR
    nsv7096791copy number variation1nstd102humanUncertain significance GRCh37 chr5: 80,083,374-80,171,681 , GRCh38.p12 chr5: 80,787,555-80,875,862 MSH3, RPS26P27
    nsv7096790copy number variation1nstd102humanPathogenic GRCh37 chr5: 79,949,868-80,074,665 , GRCh38.p12 chr5: 80,654,049-80,778,846 DHFR, MSH3
    nsv7093518insertion1nstd102humanUncertain significance GRCh37 chr5: 79,950,796-79,950,796 , GRCh38 chr5: 80,654,977-80,654,977 DHFR, MSH3
    nsv7052222inversion1nstd229human GRCh38 chr5: 80,756,630-80,756,664 , GRCh37.p13 chr5: 80,052,449-80,052,483 MSH3
    nsv7050811inversion1nstd229human GRCh38 chr5: 80,869,710-80,869,730 , GRCh37.p13 chr5: 80,165,529-80,165,549 MSH3
    nsv7049791inversion1nstd229human GRCh38 chr5: 80,727,201-81,200,159 , GRCh37.p13 chr5: 80,023,020-80,495,978 MSH3, RASGRF2-AS1, 3 more genes
    nsv7041510inversion1nstd229human GRCh38 chr5: 73,610,616-81,398,473 , GRCh37.p13 chr5: 72,906,441-80,694,292 LOC105379034, RBMX2P5, 134 more genes
    nsv6777045copy number variation1nstd229human GRCh38 chr5: 80,819,301-80,825,200 , GRCh37.p13 chr5: 80,115,120-80,121,019 MSH3
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