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 150

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098922copy number variation1nstd102humanUncertain significance GRCh38 chr20: 25,121,080-25,485,829 , GRCh37.p13 chr20: 25,101,716-25,466,465 LOC105372579, LOC100128078, 9 more genes
    nsv7096070copy number variation1nstd102humanUncertain significance GRCh37 chr20: 25,056,897-25,320,007 , GRCh38.p12 chr20: 25,076,261-25,339,371 LOC100128078, LOC284798, 7 more genes
    nsv7037094copy number variation1nstd229human GRCh38 chr20: 23,996,469-25,641,348 , GRCh37.p13 chr20: 23,977,106-25,621,984 CST7, LOC105372579, 28 more genes
    nsv7035258copy number variation1nstd229human GRCh38 chr20: 24,250,776-25,542,572 , GRCh37.p13 chr20: 24,231,412-25,523,208 LOC105372581, LINC02967, 21 more genes
    nsv7033039copy number variation1nstd229human GRCh38 chr20: 25,147,301-25,156,100 , GRCh37.p13 chr20: 25,127,937-25,136,736 LOC284798
    nsv7029182copy number variation1nstd229human GRCh38 chr20: 25,144,855-25,156,987 , GRCh37.p13 chr20: 25,125,491-25,137,623 LOC284798
    nsv7023853copy number variation1nstd229human GRCh38 chr20: 25,051,918-25,438,790 , GRCh37.p13 chr20: 25,032,554-25,419,426 PPIAP2, ACSS1, 11 more genes
    nsv6626758copy number variation1nstd224human GRCh37 chr20: 24,504,850-26,252,906 , GRCh38.p12 chr20: 24,524,214-26,272,270 NINL, PPIAP2, 39 more genes
    nsv6626682copy number variation1nstd224human GRCh37 chr20: 25,071,454-25,472,105 , GRCh38.p12 chr20: 25,090,818-25,491,469 PYGB, ABHD12, 10 more genes
    nsv6626335copy number variation1nstd224human GRCh37 chr20: 24,708,653-25,539,486 , GRCh38.p12 chr20: 24,728,017-25,558,850 ENTPD6, NINL, 17 more genes
    nsv6532719copy number variation1nstd223human GRCh38 chr20: 25,086,404-25,496,168 , GRCh37.p13 chr20: 25,067,040-25,476,804 LOC105372579, PYGB, 10 more genes
    nsv6529772copy number variation1nstd223human GRCh38 chr20: 25,111,479-25,148,245 , GRCh37.p13 chr20: 25,092,115-25,128,881 LOC284798
    nsv6520886copy number variation1nstd223human GRCh38 chr20: 24,835,426-25,188,640 , GRCh37.p13 chr20: 24,816,062-25,169,276 CST7, LOC284798, 8 more genes
    nsv6518417copy number variation1nstd223human GRCh38 chr20: 25,144,854-25,156,986 , GRCh37.p13 chr20: 25,125,490-25,137,622 LOC284798
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6134019copy number variation1nstd213human GRCh37 chr20: 25,070,000-25,500,001 , GRCh38.p12 chr20: 25,089,364-25,519,365 ENTPD6, PYGB, 10 more genes
    nsv6134018copy number variation1nstd213human GRCh37 chr20: 23,950,000-25,300,001 , GRCh38.p12 chr20: 23,969,363-25,319,365 ENTPD6, PYGB, 23 more genes
    nsv6133911copy number variation1nstd213human GRCh37 chr20: 24,530,000-25,920,001 , GRCh38.p12 chr20: 24,549,364-25,939,365 ENTPD6, NINL, 32 more genes
    nsv6133802copy number variation1nstd213human GRCh37 chr20: 24,790,000-25,220,001 , GRCh38.p12 chr20: 24,809,364-25,239,365 CST7, VSX1, 11 more genes
    nsv6133801copy number variation1nstd213human GRCh37 chr20: 24,270,000-25,770,001 , GRCh38.p12 chr20: 24,289,364-25,789,365 PYGB, CST7, 32 more genes
    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