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Items: 1 to 20 of 609

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956380insertion1nstd209human GRCh38 chr2: 166,313,008-166,313,008 , GRCh37.p13 chr2: 167,169,518-167,169,518 SCN9A
    nsv5905214copy number variation1nstd209human GRCh38 chr2: 166,299,169-166,302,282 , GRCh37.p13 chr2: 167,155,679-167,158,792 SCN1A-AS1, SCN9A
    nsv5903671copy number variation1nstd209human GRCh38 chr2: 166,201,423-166,201,594 , GRCh37.p13 chr2: 167,057,933-167,058,104 SCN1A-AS1, SCN9A
    nsv5895982copy number variation1nstd209human GRCh38 chr2: 166,200,071-166,214,621 , GRCh37.p13 chr2: 167,056,581-167,071,131 SCN9A, SCN1A-AS1
    nsv5831732copy number variation1nstd209human GRCh38 chr2: 166,201,751-166,214,317 , GRCh37.p13 chr2: 167,058,261-167,070,827 SCN9A, SCN1A-AS1
    nsv5831423copy number variation1nstd209human GRCh38 chr2: 166,299,208-166,302,311 , GRCh37.p13 chr2: 167,155,718-167,158,821 SCN9A, SCN1A-AS1
    nsv5730839mobile element insertion2nstd211human GRCh38 chr2: 166,235,403-166,235,403 , GRCh37.p13 chr2: 167,091,913-167,091,913 SCN1A-AS1, SCN9A
    nsv5716075mobile element insertion2nstd211human GRCh38 chr2: 166,311,377-166,311,377 , GRCh37.p13 chr2: 167,167,887-167,167,887 SCN9A
    nsv5682575mobile element insertion1nstd211human GRCh38 chr2: 166,290,657-166,290,657 , GRCh37.p13 chr2: 167,147,167-167,147,167 SCN1A-AS1, SCN9A
    nsv5673294copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,055,172-167,060,984 , GRCh38.p12 chr2: 166,198,662-166,204,474 SCN9A, SCN1A-AS1
    nsv5673293copy number variation1nstd102humanPathogenic GRCh37 chr2: 166,605,291-167,168,266 , GRCh38.p12 chr2: 165,748,781-166,311,756 GALNT3, SCN1A, 7 more genes
    nsv5613451insertion1nstd207human GRCh38 chr2: 166,313,008-166,313,008 , GRCh37.p13 chr2: 167,169,518-167,169,518 SCN9A
    nsv5583278copy number variation1nstd207human GRCh38 chr2: 166,299,169-166,302,282 , GRCh37.p13 chr2: 167,155,679-167,158,792 SCN9A, SCN1A-AS1
    nsv5581297copy number variation1nstd207human GRCh38 chr2: 166,201,428-166,201,543 , GRCh37.p13 chr2: 167,057,938-167,058,053 SCN1A-AS1, SCN9A
    nsv5578044copy number variation1nstd207human GRCh38 chr2: 166,222,638-166,222,968 , GRCh37.p13 chr2: 167,079,148-167,079,478 SCN1A-AS1, SCN9A
    nsv5564252copy number variation5nstd102humanPathogenic GRCh37 chr2: 165,946,660-167,168,266 , GRCh38.p12 chr2: 165,090,150-166,311,756 TTC21B-AS1, RN7SKP152, 11 more genes
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5556929mobile element insertion1nstd206human GRCh38 chr2: 166,235,403-166,235,454 , GRCh37.p13 chr2: 167,091,913-167,091,964 SCN9A, SCN1A-AS1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5539034insertion1nstd206human GRCh38 chr2: 166,346,215-166,346,223 , GRCh37.p13 chr2: 167,202,725-167,202,733 SCN9A
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