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 134

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv6738014copy number variation1nstd229human GRCh38 chr3: 138,480,262-139,118,462 , GRCh37.p13 chr3: 138,199,104-138,837,304 GAPDHP39, ATP5MC1P3, 15 more genes
    nsv6725094copy number variation1nstd229human GRCh38 chr3: 138,618,667-140,093,940 , GRCh37.p13 chr3: 138,337,509-139,812,782 RPL23AP40, FOXL2NB, 25 more genes
    nsv6720918copy number variation1nstd229human GRCh38 chr3: 138,441,482-139,164,353 , GRCh37.p13 chr3: 138,160,324-138,883,195 FAIM, ATP5MC1P3, 15 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6362129copy number variation1nstd223human GRCh38 chr3: 138,618,667-140,093,940 , GRCh37.p13 chr3: 138,337,509-139,812,782 RBP2, FAIM, 25 more genes
    nsv6311778copy number variation1nstd102humanUncertain significance GRCh37 chr3: 137,781,658-139,258,560 , GRCh38.p12 chr3: 138,062,816-139,539,718 PRR23C, ACTG1P1, 29 more genes
    nsv6134785copy number variation1nstd213human GRCh37 chr3: 135,840,000-139,360,001 , GRCh38.p12 chr3: 136,121,158-139,641,159 ACTG1P1, FOXL2, 59 more genes
    nsv5889866copy number variation1nstd209human GRCh38 chr3: 137,097,814-139,588,879 , GRCh37.p13 chr3: 136,816,656-139,307,721 , LOC105374127, 42 more genes
    nsv5453712copy number variation1nstd206human GRCh38 chr3: 139,027,574-139,067,574 , GRCh37.p13 chr3: 138,746,416-138,786,416 PRR23C
    nsv5450004copy number variation1nstd206human GRCh38 chr3: 139,043,605-139,046,526 , GRCh37.p13 chr3: 138,762,447-138,765,368 PRR23C
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034922inversion1nstd200human GRCh38 chr3: 137,979,992-148,451,901 , GRCh37.p13 chr3: 137,698,834-148,169,688 , LOC105374148, 132 more genes
    nsv4873274inversion1nstd200human GRCh37 chr3: 137,698,834-148,169,688 , GRCh38.p12 chr3: 137,979,992-148,451,901 , PLSCR5, 132 more genes
    nsv4728141copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,737,687-142,053,396 , GRCh38.p12 chr3: 139,018,845-142,334,554 RNU6-425P, YWHAQP6, 41 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4680955copy number variation1nstd189human GRCh37.p13 chr3: 138,044,866-138,867,178 , GRCh38.p12 chr3: 138,326,024-139,148,336 , FOXL2, 18 more genes
    nsv4584853copy number variation1nstd183human GRCh37 chr3: 138,305,900-138,783,114 , GRCh38.p12 chr3: 138,587,058-139,064,272 GAPDHP39, ATP5MC1P3, 12 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