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 305

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124857copy number variation1nstd186human GRCh37 chr20: 32,335,139-32,335,449 , GRCh38.p12 chr20: 33,747,333-33,747,643 ZNF341
    nsv5948967copy number variation1nstd209human GRCh38 chr20: 33,747,322-33,747,642 , GRCh37.p13 chr20: 32,335,128-32,335,448 ZNF341
    nsv5875775copy number variation1nstd209human GRCh38 chr20: 33,769,763-33,794,418 , GRCh37.p13 chr20: 32,357,569-32,382,224 ZNF341, ZNF341-AS1
    nsv5586066copy number variation1nstd207human GRCh38 chr20: 33,747,322-33,747,642 , GRCh37.p13 chr20: 32,335,128-32,335,448 ZNF341
    nsv5533712copy number variation1nstd206human GRCh38 chr20: 33,737,470-33,744,730 , GRCh37.p13 chr20: 32,325,276-32,332,536 ZNF341
    nsv5529071copy number variation1nstd206human GRCh38 chr20: 33,760,801-33,764,315 , GRCh37.p13 chr20: 32,348,607-32,352,121 ZNF341
    nsv5526013copy number variation1nstd206human GRCh38 chr20: 33,792,734-33,796,019 , GRCh37.p13 chr20: 32,380,540-32,383,825 ZNF341, ZNF341-AS1
    nsv5521569copy number variation1nstd206human GRCh38 chr20: 33,747,333-33,747,643 , GRCh37.p13 chr20: 32,335,139-32,335,449 ZNF341
    nsv5518436copy number variation1nstd206human GRCh38 chr20: 33,770,848-33,777,339 , GRCh37.p13 chr20: 32,358,654-32,365,145 ZNF341
    nsv5384631mobile element deletion2nstd186human GRCh37 chr20: 32,335,139-32,335,449 , GRCh38.p12 chr20: 33,747,333-33,747,643 ZNF341
    nsv5283490copy number variation1nstd204human GRCh38.p13 chr20: 33,726,814-33,732,813 , GRCh37.p13 chr20: 32,314,620-32,320,619 ZNF341
    nsv5208980mobile element deletion1nstd204human GRCh38.p13 chr20: 33,747,330-33,747,645 , GRCh37.p13 chr20: 32,335,136-32,335,451 ZNF341
    nsv5182397mobile element insertion1nstd203human GRCh38 chr20: 33,752,516-33,752,534 , GRCh37.p13 chr20: 32,340,322-32,340,340 ZNF341, RPL31P2
    nsv5174000mobile element insertion1nstd203human GRCh38 chr20: 33,761,061-33,761,061 , GRCh37.p13 chr20: 32,348,867-32,348,867 ZNF341
    nsv5166402mobile element insertion1nstd203human GRCh38 chr20: 33,764,561-33,764,590 , GRCh37.p13 chr20: 32,352,367-32,352,396 ZNF341
    nsv5160482mobile element insertion1nstd203human GRCh38 chr20: 33,764,590-33,764,604 , GRCh37.p13 chr20: 32,352,396-32,352,410 ZNF341
    nsv5022398copy number variation1nstd200human GRCh38 chr20: 33,792,708-33,796,021 , GRCh37.p13 chr20: 32,380,514-32,383,827 ZNF341-AS1, ZNF341
    nsv5022397copy number variation1nstd200human GRCh38 chr20: 33,755,042-33,760,582 , GRCh37.p13 chr20: 32,342,848-32,348,388 ZNF341
    nsv5022396copy number variation1nstd200human GRCh38 chr20: 33,753,012-33,754,643 , GRCh37.p13 chr20: 32,340,818-32,342,449 ZNF341, RPL31P2
    nsv5022395copy number variation1nstd200human GRCh38 chr20: 33,742,337-33,743,384 , GRCh37.p13 chr20: 32,330,143-32,331,190 ZNF341
    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