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Items: 1 to 20 of 1354

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5979034inversion1nstd209human GRCh38 chr4: 136,299,558-138,570,240 , GRCh37.p13 chr4: 137,220,713-139,491,394 SLC7A11, PCDH18, 20 more genes
    nsv5963631insertion1nstd209human GRCh38 chr4: 136,975,627-136,975,627 , GRCh37.p13 chr4: 137,896,781-137,896,781 LINC02511
    nsv5962866insertion1nstd209human GRCh38 chr4: 137,164,739-137,164,739 , GRCh37.p13 chr4: 138,085,893-138,085,893 LINC02511
    nsv5962000insertion1nstd209human GRCh38 chr4: 137,148,044-137,148,044 , GRCh37.p13 chr4: 138,069,198-138,069,198 LINC02511
    nsv5960823insertion1nstd209human GRCh38 chr4: 137,030,084-137,030,084 , GRCh37.p13 chr4: 137,951,238-137,951,238 LINC02511
    nsv5959971insertion1nstd209human GRCh38 chr4: 136,848,195-136,848,195 , GRCh37.p13 chr4: 137,769,349-137,769,349 LINC02511
    nsv5954187insertion1nstd209human GRCh38 chr4: 136,885,361-136,885,361 , GRCh37.p13 chr4: 137,806,515-137,806,515 LINC02511
    nsv5906827copy number variation1nstd209human GRCh38 chr4: 137,170,846-137,179,476 , GRCh37.p13 chr4: 138,092,000-138,100,630 LINC02511
    nsv5897799copy number variation1nstd209human GRCh38 chr4: 137,168,740-137,168,817 , GRCh37.p13 chr4: 138,089,894-138,089,971 LINC02511
    nsv5897274copy number variation1nstd209human GRCh38 chr4: 137,022,849-137,022,975 , GRCh37.p13 chr4: 137,944,003-137,944,129 LINC02511
    nsv5892039copy number variation1nstd209human GRCh38 chr4: 137,079,888-137,079,955 , GRCh37.p13 chr4: 138,001,042-138,001,109 LINC02511
    nsv5890182copy number variation1nstd209human GRCh38 chr4: 137,051,325-137,065,868 , GRCh37.p13 chr4: 137,972,479-137,987,022 LINC02511
    nsv5838255copy number variation1nstd209human GRCh38 chr4: 137,170,914-137,179,379 , GRCh37.p13 chr4: 138,092,068-138,100,533 LINC02511
    nsv5837989copy number variation1nstd209human GRCh38 chr4: 136,863,515-136,865,514 , GRCh37.p13 chr4: 137,784,669-137,786,668 LINC02511
    nsv5837705copy number variation1nstd209human GRCh38 chr4: 137,053,638-137,064,612 , GRCh37.p13 chr4: 137,974,792-137,985,766 LINC02511
    nsv5721109mobile element insertion1nstd211human GRCh38 chr4: 136,973,775-136,973,775 , GRCh37.p13 chr4: 137,894,929-137,894,929 LINC02511
    nsv5719614mobile element insertion1nstd211human GRCh38 chr4: 137,105,211-137,105,211 , GRCh37.p13 chr4: 138,026,365-138,026,365 LINC02511
    nsv5689703mobile element insertion2nstd211human GRCh38 chr4: 136,944,900-136,944,900 , GRCh37.p13 chr4: 137,866,054-137,866,054 LINC02511
    nsv5688511mobile element insertion2nstd211human GRCh38 chr4: 136,959,425-136,959,425 , GRCh37.p13 chr4: 137,880,579-137,880,579 LINC02511
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