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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5886317copy number variation1nstd209human GRCh38 chr1: 247,416,614-247,416,676 , GRCh37.p13 chr1: 247,579,916-247,579,978 NLRP3
    nsv5877048copy number variation1nstd209human GRCh38 chr1: 247,433,890-247,433,973 , GRCh37.p13 chr1: 247,597,192-247,597,275 NLRP3
    nsv5867757copy number variation1nstd209human GRCh38 chr1: 247,427,996-247,428,068 , GRCh37.p13 chr1: 247,591,298-247,591,370 NLRP3
    nsv5618399insertion1nstd207human GRCh38 chr1: 247,416,614-247,416,614 , GRCh37.p13 chr1: 247,579,916-247,579,916 NLRP3
    nsv5614970insertion1nstd207human GRCh38 chr1: 247,433,963-247,433,963 , GRCh37.p13 chr1: 247,597,265-247,597,265 NLRP3
    nsv5614771insertion1nstd207human GRCh38 chr1: 247,427,581-247,427,581 , GRCh37.p13 chr1: 247,590,883-247,590,883 NLRP3
    nsv5610917insertion1nstd207human GRCh38 chr1: 247,428,182-247,428,182 , GRCh37.p13 chr1: 247,591,484-247,591,484 NLRP3
    nsv5582790copy number variation1nstd207human GRCh38 chr1: 247,416,614-247,416,676 , GRCh37.p13 chr1: 247,579,916-247,579,978 NLRP3
    nsv5574339copy number variation1nstd207human GRCh38 chr1: 247,433,890-247,433,973 , GRCh37.p13 chr1: 247,597,192-247,597,275 NLRP3
    nsv5570017copy number variation1nstd207human GRCh38 chr1: 247,433,769-247,433,978 , GRCh37.p13 chr1: 247,597,071-247,597,280 NLRP3
    nsv5568827copy number variation1nstd207human GRCh38 chr1: 247,427,595-247,427,740 , GRCh37.p13 chr1: 247,590,897-247,591,042 NLRP3
    nsv5438953copy number variation1nstd206human GRCh38 chr1: 247,447,717-247,447,783 , GRCh37.p13 chr1: 247,611,019-247,611,085 NLRP3
    nsv5382975copy number variation2nstd186human GRCh37 chr1: 247,596,886-247,597,375 , GRCh38.p12 chr1: 247,433,584-247,434,073 NLRP3
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5381215copy number variation1nstd102humanUncertain significance GRCh37 chr1: 247,607,254-247,617,036 , GRCh38.p12 chr1: 247,443,952-247,453,734 NLRP3, OR2B11
    nsv4904622copy number variation1nstd200human GRCh38 chr1: 247,433,584-247,434,073 , GRCh37.p13 chr1: 247,596,886-247,597,375 NLRP3
    nsv4891846copy number variation1nstd200human GRCh38 chr1: 247,395,535-247,429,084 , GRCh37.p13 chr1: 247,558,837-247,592,386 NLRP3
    nsv4870022inversion1nstd200human GRCh37 chr1: 247,517,183-247,641,595 , GRCh38.p12 chr1: 247,353,881-247,478,293 NLRP3, OR2B11, 2 more genes
    nsv4788170copy number variation1nstd200human GRCh37 chr1: 247,596,886-247,597,375 , GRCh38.p12 chr1: 247,433,584-247,434,073 NLRP3
    nsv4785772copy number variation1nstd200human GRCh37 chr1: 247,558,837-247,592,386 , GRCh38.p12 chr1: 247,395,535-247,429,084 NLRP3
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