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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131746insertion1nstd186human GRCh37 chr20: 18,530,750-18,530,759 , GRCh38.p12 chr20: 18,550,106-18,550,115 SEC23B
    nsv5716535mobile element insertion2nstd211human GRCh38 chr20: 18,552,197-18,552,197 , GRCh37.p13 chr20: 18,532,841-18,532,841 SEC23B
    nsv5708099mobile element insertion2nstd211human GRCh38 chr20: 18,552,197-18,552,197 , GRCh37.p13 chr20: 18,532,841-18,532,841 SEC23B
    nsv5555728mobile element insertion1nstd206human GRCh38 chr20: 18,552,197-18,552,248 , GRCh37.p13 chr20: 18,532,841-18,532,892 SEC23B
    nsv5543282insertion1nstd206human GRCh38 chr20: 18,527,655-18,527,688 , GRCh37.p13 chr20: 18,508,299-18,508,332 SEC23B
    nsv5538265insertion1nstd206human GRCh38 chr20: 18,550,106-18,550,115 , GRCh37.p13 chr20: 18,530,750-18,530,759 SEC23B
    nsv5514994copy number variation1nstd206human GRCh38 chr20: 18,534,404-18,534,501 , GRCh37.p13 chr20: 18,515,048-18,515,145 SEC23B
    nsv5182431mobile element insertion1nstd203human GRCh38 chr20: 18,552,183-18,552,197 , GRCh37.p13 chr20: 18,532,827-18,532,841 SEC23B
    nsv5168730mobile element insertion1nstd203human GRCh38 chr20: 18,542,799-18,542,812 , GRCh37.p13 chr20: 18,523,443-18,523,456 SEC23B
    nsv5166613mobile element insertion1nstd203human GRCh38 chr20: 18,558,827-18,558,843 , GRCh37.p13 chr20: 18,539,471-18,539,487 SEC23B
    nsv5162436mobile element insertion1nstd203human GRCh38 chr20: 18,518,605-18,518,609 , GRCh37.p13 chr20: 18,499,249-18,499,253 SEC23B
    nsv5025182copy number variation1nstd200human GRCh38 chr20: 18,526,038-18,534,805 , GRCh37.p13 chr20: 18,506,682-18,515,449 SEC23B
    nsv5021586copy number variation1nstd200human GRCh38 chr20: 18,553,292-18,553,393 , GRCh37.p13 chr20: 18,533,936-18,534,037 SEC23B
    nsv5021585copy number variation1nstd200human GRCh38 chr20: 18,536,508-18,539,047 , GRCh37.p13 chr20: 18,517,152-18,519,691 SEC23B
    nsv5021584copy number variation1nstd200human GRCh38 chr20: 18,532,251-18,532,371 , GRCh37.p13 chr20: 18,512,895-18,513,015 SEC23B
    nsv5021583copy number variation1nstd200human GRCh38 chr20: 18,511,406-18,520,977 , GRCh37.p13 chr20: 18,492,050-18,501,621 SEC23B
    nsv4684075copy number variation2nstd102humanPathogenic GRCh37 chr20: 18,492,869-18,496,380 , GRCh38.p12 chr20: 18,512,225-18,515,736 SEC23B
    nsv4680344copy number variation1nstd189human GRCh37.p13 chr20: 18,175,953-18,491,407 , GRCh38.p12 chr20: 18,195,309-18,510,763 ZNF133, SEC23B, 17 more genes
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4634280copy number variation1nstd183human GRCh37 chr20: 18,208,790-19,102,422 , GRCh38.p12 chr20: 18,228,146-19,121,778 , RNA5SP476, 30 more genes
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