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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955677insertion1nstd209human GRCh38 chr5: 179,748,397-179,748,397 , GRCh37.p13 chr5: 179,175,398-179,175,398 MAML1
    nsv5947946insertion1nstd209human GRCh38 chr5: 179,752,341-179,752,341 , GRCh37.p13 chr5: 179,179,342-179,179,342 MAML1
    nsv5893429copy number variation1nstd209human GRCh38 chr5: 179,737,781-179,737,862 , GRCh37.p13 chr5: 179,164,782-179,164,863 MAML1
    nsv5689693mobile element insertion2nstd211human GRCh38 chr5: 179,748,412-179,748,412 , GRCh37.p13 chr5: 179,175,413-179,175,413 MAML1
    nsv5686759mobile element insertion2nstd211human GRCh38 chr5: 179,755,547-179,755,547 , GRCh37.p13 chr5: 179,182,548-179,182,548 MAML1
    nsv5641347insertion1nstd207human GRCh38 chr5: 179,737,781-179,737,781 , GRCh37.p13 chr5: 179,164,782-179,164,782 MAML1
    nsv5632179insertion1nstd207human GRCh38 chr5: 179,748,397-179,748,397 , GRCh37.p13 chr5: 179,175,398-179,175,398 MAML1
    nsv5626038insertion1nstd207human GRCh38 chr5: 179,764,880-179,764,880 , GRCh37.p13 chr5: 179,191,881-179,191,881 MAML1
    nsv5561640sequence alteration1nstd206human GRCh38 chr5: 179,554,688-180,310,132 , GRCh37.p13 chr5: 178,981,689-179,737,132 LTC4S, MIR340, 28 more genes
    nsv5468757copy number variation1nstd206human GRCh38 chr5: 179,751,170-179,753,004 , GRCh37.p13 chr5: 179,178,171-179,180,005 MAML1
    nsv5460406copy number variation1nstd206human GRCh38 chr5: 179,737,781-179,737,863 , GRCh37.p13 chr5: 179,164,782-179,164,864 MAML1
    nsv5460163copy number variation1nstd206human GRCh38 chr5: 179,764,703-179,764,901 , GRCh37.p13 chr5: 179,191,704-179,191,902 MAML1
    nsv5457618copy number variation1nstd206human GRCh38 chr5: 179,746,387-179,748,146 , GRCh37.p13 chr5: 179,173,388-179,175,147 MAML1
    nsv5402215mobile element insertion1nstd206human GRCh38 chr5: 179,755,547-179,755,593 , GRCh37.p13 chr5: 179,182,548-179,182,594 MAML1
    nsv5381440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,699,902-179,263,603 , GRCh38.p12 chr5: 179,272,901-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 37,608-602,163 LOC105377762, LOC105377759, 21 more genes
    nsv5381377copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,770,758-179,263,603 , GRCh38.p12 chr5: 179,343,757-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 108,464-602,163 LOC100502572, C5orf60, 21 more genes
    nsv5301596copy number variation1nstd204human GRCh38.p13 chr5: 179,616,292-180,442,361 , GRCh37.p13 chr5: 179,043,293-179,869,361 MIR1229, MAPK9, 25 more genes
    nsv5238795copy number variation1nstd204human GRCh37.p13 chr5: 179,084,702-179,213,801 , GRCh38.p13 chr5: 179,657,701-179,786,800 CANX, MAML1, 4 more genes
    nsv5238439copy number variation1nstd204human GRCh38.p13 chr5: 179,763,766-179,771,576 , GRCh37.p13 chr5: 179,190,767-179,198,577 MAML1
    nsv5238201copy number variation1nstd204human GRCh38.p13 chr5: 179,741,901-179,754,300 , GRCh37.p13 chr5: 179,168,902-179,181,301 MAML1
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