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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114835mobile element insertion1nstd186human GRCh37 chr16: 50,760,156-50,760,156 , GRCh38.p12 chr16: 50,726,245-50,726,245 NOD2
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5969568insertion1nstd209human GRCh38 chr16: 50,726,245-50,726,245 , GRCh37.p13 chr16: 50,760,156-50,760,156 NOD2
    nsv5703225mobile element insertion2nstd211human GRCh38 chr16: 50,726,256-50,726,256 , GRCh37.p13 chr16: 50,760,167-50,760,167 NOD2
    nsv5647983insertion1nstd207human GRCh38 chr16: 50,726,245-50,726,245 , GRCh37.p13 chr16: 50,760,156-50,760,156 NOD2
    nsv5587815copy number variation1nstd207human GRCh38 chr16: 50,693,036-50,693,275 , GRCh37.p13 chr16: 50,726,947-50,727,186 NOD2
    nsv5524165copy number variation1nstd206human GRCh38 chr16: 50,654,254-50,854,695 , GRCh37.p13 chr16: 50,688,165-50,888,606 CYLD, NOD2, 6 more genes
    nsv5514984copy number variation1nstd206human GRCh38 chr16: 50,693,031-50,693,296 , GRCh37.p13 chr16: 50,726,942-50,727,207 NOD2
    nsv5425595mobile element insertion1nstd206human GRCh38 chr16: 50,726,245-50,726,245 , GRCh37.p13 chr16: 50,760,156-50,760,156 NOD2
    nsv5345764translocation1nstd200human GRCh37 chr16: 50,740,678-50,740,678 , GRCh37 chr16: 58,719,844-58,719,844 , GRCh38.p12 chr16: 50,706,767-50,706,767 , GRCh38.p12 chr16: 58,685,940-58,685,940 NOD2
    nsv5155414mobile element insertion1nstd203human GRCh38 chr16: 50,701,635-50,701,650 , GRCh37.p13 chr16: 50,735,546-50,735,561 NOD2
    nsv5154893mobile element insertion1nstd203human GRCh38 chr16: 50,692,167-50,692,167 , GRCh37.p13 chr16: 50,726,078-50,726,078 NOD2
    nsv5153174mobile element insertion1nstd203human GRCh38 chr16: 50,726,252-50,726,256 , GRCh37.p13 chr16: 50,760,163-50,760,167 NOD2
    nsv5142633mobile element insertion1nstd203human GRCh38 chr16: 50,726,245-50,726,256 , GRCh37.p13 chr16: 50,760,156-50,760,167 NOD2
    nsv5142055mobile element insertion1nstd203human GRCh38 chr16: 50,726,250-50,726,256 , GRCh37.p13 chr16: 50,760,161-50,760,167 NOD2
    nsv5004082copy number variation1nstd200human GRCh38 chr16: 50,692,360-50,700,685 , GRCh37.p13 chr16: 50,726,271-50,734,596 NOD2
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4718858insertion1nstd186human GRCh37 chr16: 50,760,156-50,760,156 , GRCh38.p12 chr16: 50,726,245-50,726,245 NOD2
    nsv4702776copy number variation1nstd195human GRCh37 chr16: 50,383,251-51,282,851 , GRCh38.p12 chr16: 50,349,340-51,248,940 , BRD7, 18 more genes
    nsv4547272insertion1nstd166human GRCh37.p13 chr16: 50,760,156-50,760,156 , GRCh38.p12 chr16: 50,726,245-50,726,245 NOD2
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