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Items: 1 to 20 of 321

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922607copy number variation1nstd209human GRCh38 chr11: 35,691,866-35,696,407 , GRCh37.p13 chr11: 35,713,414-35,717,955 TRIM44
    nsv5920322copy number variation1nstd209human GRCh38 chr11: 35,800,459-35,800,524 , GRCh37.p13 chr11: 35,822,009-35,822,074 TRIM44
    nsv5910903copy number variation1nstd209human GRCh38 chr11: 35,752,483-35,752,601 , GRCh37.p13 chr11: 35,774,031-35,774,149 TRIM44
    nsv5865474copy number variation1nstd209human GRCh38 chr11: 35,691,897-35,696,246 , GRCh37.p13 chr11: 35,713,445-35,717,794 TRIM44
    nsv5722369mobile element insertion1nstd211human GRCh38 chr11: 35,762,253-35,762,253 , GRCh37.p13 chr11: 35,783,801-35,783,801 TRIM44
    nsv5721030mobile element insertion1nstd211human GRCh38 chr11: 35,732,460-35,732,460 , GRCh37.p13 chr11: 35,754,008-35,754,008 TRIM44
    nsv5719460mobile element insertion2nstd211human GRCh38 chr11: 35,802,010-35,802,010 , GRCh37.p13 chr11: 35,823,560-35,823,560 TRIM44
    nsv5717231mobile element insertion1nstd211human GRCh38 chr11: 35,814,850-35,814,850 , GRCh37.p13 chr11: 35,836,400-35,836,400 TRIM44
    nsv5713568mobile element insertion1nstd211human GRCh38 chr11: 35,749,338-35,749,338 , GRCh37.p13 chr11: 35,770,886-35,770,886 TRIM44
    nsv5713381mobile element insertion2nstd211human GRCh38 chr11: 35,673,221-35,673,221 , GRCh37.p13 chr11: 35,694,769-35,694,769 TRIM44
    nsv5710236mobile element insertion1nstd211human GRCh38 chr11: 35,686,356-35,686,356 , GRCh37.p13 chr11: 35,707,904-35,707,904 TRIM44
    nsv5651080insertion1nstd207human GRCh38 chr11: 35,708,526-35,708,526 , GRCh37.p13 chr11: 35,730,074-35,730,074 TRIM44
    nsv5510120copy number variation1nstd206human GRCh38 chr11: 35,667,124-35,667,279 , GRCh37.p13 chr11: 35,688,672-35,688,827 TRIM44
    nsv5510044copy number variation1nstd206human GRCh38 chr11: 35,691,850-35,696,338 , GRCh37.p13 chr11: 35,713,398-35,717,886 TRIM44
    nsv5501987copy number variation1nstd206human GRCh38 chr11: 35,752,485-35,752,602 , GRCh37.p13 chr11: 35,774,033-35,774,150 TRIM44
    nsv5496449copy number variation1nstd206human GRCh38 chr11: 35,699,850-35,707,000 , GRCh37.p13 chr11: 35,721,398-35,728,548 TRIM44
    nsv5495207copy number variation1nstd206human GRCh38 chr11: 35,740,452-35,744,025 , GRCh37.p13 chr11: 35,762,000-35,765,573 TRIM44
    nsv5402619mobile element insertion1nstd206human GRCh38 chr11: 35,673,221-35,673,272 , GRCh37.p13 chr11: 35,694,769-35,694,820 TRIM44
    nsv5398708mobile element insertion1nstd206human GRCh38 chr11: 35,749,338-35,749,389 , GRCh37.p13 chr11: 35,770,886-35,770,937 TRIM44
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
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