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Items: 1 to 20 of 942

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147682insertion1nstd232human GRCh37.p13 chr1: 3,495,309-3,495,309 , GRCh38.p12 chr1: 3,578,745-3,578,745 MEGF6
    nsv7146068copy number variation1nstd232human GRCh37.p13 chr1: 3,488,273-3,488,329 , GRCh38.p12 chr1: 3,571,709-3,571,765 MEGF6
    nsv7145133insertion1nstd232human GRCh37.p13 chr1: 3,418,581-3,418,581 , GRCh38.p12 chr1: 3,502,017-3,502,017 MEGF6
    nsv7140456insertion1nstd232human GRCh37.p13 chr1: 3,495,346-3,495,346 , GRCh38.p12 chr1: 3,578,782-3,578,782 MEGF6
    nsv7138450copy number variation1nstd232human GRCh37.p13 chr1: 3,508,320-3,508,385 , GRCh38.p12 chr1: 3,591,756-3,591,821 MEGF6
    nsv7137191copy number variation1nstd102humanPathogenic GRCh37 chr1: 1,957,148-6,553,454 , GRCh38.p12 chr1: 2,025,709-6,493,394 LOC102724429, TNFRSF14, 86 more genes
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099173copy number variation1nstd231human GRCh38.p12 chr1: 3,521,699-3,692,482 , GRCh37 chr1: 3,438,263-3,609,046 MEGF6, TP73, 5 more genes
    nsv7099172copy number variation1nstd231human GRCh38.p12 chr1: 3,353,612-3,503,571 , GRCh37 chr1: 3,270,176-3,420,135 MEGF6, ARHGEF16, 1 more genes
    nsv7098948copy number variation1nstd102humanUncertain significance GRCh38 chr1: 2,518,272-4,413,203 , GRCh37.p13 chr1: 2,449,711-4,473,263 LOC107984904, DFFB, 46 more genes
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 more genes
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7051203inversion1nstd229human GRCh38 chr1: 2,476,867-3,696,891 , GRCh37.p13 chr1: 2,408,306-3,613,455 TP73, PRXL2B, 33 more genes
    nsv7046684inversion1nstd229human GRCh38 chr1: 3,604,438-3,606,892 , GRCh37.p13 chr1: 3,521,002-3,523,456 MEGF6
    nsv7042148inversion1nstd229human GRCh38 chr1: 3,616,757-3,620,417 , GRCh37.p13 chr1: 3,533,321-3,536,981 MEGF6
    nsv7041929inversion1nstd229human GRCh38 chr1: 3,491,360-3,495,048 , GRCh37.p13 chr1: 3,407,924-3,411,612 MEGF6
    nsv7039579inversion1nstd229human GRCh38 chr1: 3,547,818-3,550,111 , GRCh37.p13 chr1: 3,464,382-3,466,675 MEGF6, LOC105378608
    nsv6649467copy number variation1nstd229human GRCh38 chr1: 3,612,271-3,612,361 , GRCh37.p13 chr1: 3,528,835-3,528,925 MEGF6
    nsv6649457copy number variation1nstd229human GRCh38 chr1: 3,585,078-3,586,302 , GRCh37.p13 chr1: 3,501,642-3,502,866 MEGF6
    nsv6649456copy number variation1nstd229human GRCh38 chr1: 3,585,036-3,585,254 , GRCh37.p13 chr1: 3,501,600-3,501,818 MEGF6
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