U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 131

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925518copy number variation1nstd209human GRCh38 chr11: 62,780,684-62,780,989 , GRCh37.p13 chr11: 62,548,156-62,548,461 TAF6L
    nsv5715351mobile element insertion1nstd211human GRCh38 chr11: 62,779,683-62,779,683 , GRCh37.p13 chr11: 62,547,155-62,547,155 TAF6L
    nsv5650908insertion1nstd207human GRCh38 chr11: 62,784,008-62,784,008 , GRCh37.p13 chr11: 62,551,480-62,551,480 TAF6L
    nsv5513625copy number variation1nstd206human GRCh38 chr11: 62,765,000-62,773,200 , GRCh37.p13 chr11: 62,532,472-62,540,672 POLR2G, TAF6L
    nsv5508254copy number variation1nstd206human GRCh38 chr11: 62,783,556-62,785,087 , GRCh37.p13 chr11: 62,551,028-62,552,559 TAF6L
    nsv5501978copy number variation1nstd206human GRCh38 chr11: 62,783,504-62,783,753 , GRCh37.p13 chr11: 62,550,976-62,551,225 TAF6L
    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
    nsv5316971copy number variation1nstd204human GRCh38.p13 chr11: 62,774,181-62,784,049 , GRCh37.p13 chr11: 62,541,653-62,551,521 TAF6L
    nsv5313232copy number variation1nstd204human GRCh38.p13 chr11: 62,779,322-62,784,055 , GRCh37.p13 chr11: 62,546,794-62,551,527 TAF6L
    nsv5275128copy number variation1nstd204human GRCh38.p13 chr11: 62,779,301-62,784,200 , GRCh37.p13 chr11: 62,546,773-62,551,672 TAF6L
    nsv5273551copy number variation1nstd204human GRCh38.p13 chr11: 62,779,209-62,783,856 , GRCh37.p13 chr11: 62,546,681-62,551,328 TAF6L
    nsv5272897copy number variation1nstd204human GRCh38.p13 chr11: 62,779,334-62,780,558 , GRCh37.p13 chr11: 62,546,806-62,548,030 TAF6L
    nsv5268235copy number variation1nstd204human GRCh38.p13 chr11: 62,664,401-62,843,200 , GRCh37.p13 chr11: 62,431,873-62,610,672 HNRNPUL2, UQCC3, 23 more genes
    nsv5267546copy number variation1nstd204human GRCh38.p13 chr11: 62,769,624-62,778,683 , GRCh37.p13 chr11: 62,537,096-62,546,155 TAF6L
    nsv5267101copy number variation1nstd204human GRCh38.p13 chr11: 62,774,004-62,783,993 , GRCh37.p13 chr11: 62,541,476-62,551,465 TAF6L
    nsv5266012copy number variation1nstd204human GRCh38.p13 chr11: 62,774,201-62,784,100 , GRCh37.p13 chr11: 62,541,673-62,551,572 TAF6L
    nsv5260849copy number variation1nstd204human GRCh38.p13 chr11: 62,773,029-62,774,433 , GRCh37.p13 chr11: 62,540,501-62,541,905 TAF6L
    nsv5133244mobile element insertion1nstd203human GRCh38 chr11: 62,780,749-62,780,789 , GRCh37.p13 chr11: 62,548,221-62,548,261 TAF6L
    nsv4985020copy number variation1nstd200human GRCh38 chr11: 62,770,353-62,773,725 , GRCh37.p13 chr11: 62,537,825-62,541,197 TAF6L
    nsv4979718copy number variation1nstd200human GRCh38 chr11: 62,779,331-62,784,094 , GRCh37.p13 chr11: 62,546,803-62,551,566 TAF6L
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center