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 353

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978758insertion1nstd209human GRCh38 chr12: 25,085,739-25,085,739 , GRCh37.p13 chr12: 25,238,673-25,238,673 IRAG2
    nsv5978437insertion1nstd209human GRCh38 chr12: 25,100,000-25,100,000 , GRCh37.p13 chr12: 25,252,934-25,252,934 IRAG2
    nsv5977327insertion1nstd209human GRCh38 chr12: 25,077,275-25,077,275 , GRCh37.p13 chr12: 25,230,209-25,230,209 IRAG2
    nsv5977239insertion1nstd209human GRCh38 chr12: 25,106,528-25,106,528 , GRCh37.p13 chr12: 25,259,462-25,259,462 IRAG2, DNAI7
    nsv5923742copy number variation1nstd209human GRCh38 chr12: 21,398,810-28,763,815 , GRCh37.p13 chr12: 21,551,744-28,916,748 , LOC105369710, 101 more genes
    nsv5916901copy number variation1nstd209human GRCh38 chr12: 21,398,719-28,763,765 , GRCh37.p13 chr12: 21,551,653-28,916,698 , LOC105369704, 101 more genes
    nsv5864596copy number variation1nstd209human GRCh38 chr12: 25,066,573-25,067,872 , GRCh37.p13 chr12: 25,219,507-25,220,806 IRAG2
    nsv5706539mobile element insertion2nstd211human GRCh38 chr12: 25,089,835-25,089,835 , GRCh37.p13 chr12: 25,242,769-25,242,769 IRAG2
    nsv5661593insertion1nstd207human GRCh38 chr12: 25,106,528-25,106,528 , GRCh37.p13 chr12: 25,259,462-25,259,462 IRAG2, DNAI7
    nsv5660943insertion1nstd207human GRCh38 chr12: 25,085,739-25,085,739 , GRCh37.p13 chr12: 25,238,673-25,238,673 IRAG2
    nsv5659215insertion1nstd207human GRCh38 chr12: 25,077,286-25,077,286 , GRCh37.p13 chr12: 25,230,220-25,230,220 IRAG2
    nsv5655321insertion1nstd207human GRCh38 chr12: 25,077,273-25,077,273 , GRCh37.p13 chr12: 25,230,207-25,230,207 IRAG2
    nsv5653839insertion1nstd207human GRCh38 chr12: 25,077,374-25,077,374 , GRCh37.p13 chr12: 25,230,308-25,230,308 IRAG2
    nsv5653137insertion1nstd207human GRCh38 chr12: 25,077,360-25,077,360 , GRCh37.p13 chr12: 25,230,294-25,230,294 IRAG2
    nsv5550477insertion1nstd206human GRCh38 chr12: 25,106,528-25,106,528 , GRCh37.p13 chr12: 25,259,462-25,259,462 DNAI7, IRAG2
    nsv5547293insertion1nstd206human GRCh38 chr12: 25,085,753-25,085,790 , GRCh37.p13 chr12: 25,238,687-25,238,724 IRAG2
    nsv5505426copy number variation1nstd206human GRCh38 chr12: 25,053,678-25,053,825 , GRCh37.p13 chr12: 25,206,612-25,206,759 IRAG2
    nsv5496407copy number variation1nstd206human GRCh38 chr12: 25,091,497-25,091,972 , GRCh37.p13 chr12: 25,244,431-25,244,906 IRAG2, CENPUP2
    nsv5416103mobile element insertion1nstd206human GRCh38 chr12: 25,089,835-25,089,842 , GRCh37.p13 chr12: 25,242,769-25,242,776 IRAG2
    nsv5132856mobile element insertion1nstd203human GRCh38 chr12: 25,089,820-25,089,833 , GRCh37.p13 chr12: 25,242,754-25,242,767 IRAG2
    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