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 378

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963362insertion1nstd209human GRCh38 chr10: 91,260,116-91,260,116 , GRCh37.p13 chr10: 93,019,873-93,019,873 PCGF5
    nsv5922466copy number variation1nstd209human GRCh38 chr10: 91,209,468-91,209,805 , GRCh37.p13 chr10: 92,969,225-92,969,562 PCGF5
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5917454copy number variation1nstd209human GRCh38 chr10: 91,225,199-91,225,286 , GRCh37.p13 chr10: 92,984,956-92,985,043 PCGF5
    nsv5710518mobile element insertion1nstd211human GRCh38 chr10: 91,209,801-91,209,801 , GRCh37.p13 chr10: 92,969,558-92,969,558 PCGF5
    nsv5708950mobile element insertion1nstd211human GRCh38 chr10: 91,230,333-91,230,333 , GRCh37.p13 chr10: 92,990,090-92,990,090 PCGF5
    nsv5705620mobile element insertion1nstd211human GRCh38 chr10: 91,269,457-91,269,457 , GRCh37.p13 chr10: 93,029,214-93,029,214 PCGF5
    nsv5639774insertion1nstd207human GRCh38 chr10: 91,260,116-91,260,116 , GRCh37.p13 chr10: 93,019,873-93,019,873 PCGF5
    nsv5632190insertion1nstd207human GRCh38 chr10: 91,269,444-91,269,444 , GRCh37.p13 chr10: 93,029,201-93,029,201 PCGF5
    nsv5602776copy number variation1nstd207human GRCh38 chr10: 91,209,468-91,209,805 , GRCh37.p13 chr10: 92,969,225-92,969,562 PCGF5
    nsv5543521insertion1nstd206human GRCh38 chr10: 91,260,133-91,260,167 , GRCh37.p13 chr10: 93,019,890-93,019,924 PCGF5
    nsv5493683copy number variation1nstd206human GRCh38 chr10: 91,240,909-91,243,515 , GRCh37.p13 chr10: 93,000,666-93,003,272 PCGF5
    nsv5486571copy number variation1nstd206human GRCh38 chr10: 91,168,647-91,168,743 , GRCh37.p13 chr10: 92,928,404-92,928,500 PCGF5
    nsv5485657copy number variation1nstd206human GRCh38 chr10: 91,250,164-91,250,228 , GRCh37.p13 chr10: 93,009,921-93,009,985 PCGF5
    nsv5483682copy number variation1nstd206human GRCh38 chr10: 91,228,110-91,232,360 , GRCh37.p13 chr10: 92,987,867-92,992,117 PCGF5
    nsv5483247copy number variation1nstd206human GRCh38 chr10: 91,164,766-91,174,113 , GRCh37.p13 chr10: 92,924,523-92,933,870 PCGF5
    nsv5480919copy number variation1nstd206human GRCh38 chr10: 91,209,474-91,209,806 , GRCh37.p13 chr10: 92,969,231-92,969,563 PCGF5
    nsv5474265copy number variation1nstd206human GRCh38 chr10: 91,226,277-91,234,595 , GRCh37.p13 chr10: 92,986,034-92,994,352 PCGF5
    nsv5394340mobile element insertion1nstd206human GRCh38 chr10: 91,269,457-91,269,508 , GRCh37.p13 chr10: 93,029,214-93,029,265 PCGF5
    nsv5383941mobile element deletion1nstd186human GRCh37 chr10: 92,969,231-92,969,563 , GRCh38.p12 chr10: 91,209,474-91,209,806 PCGF5
    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