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 239

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055821inversion1nstd229human GRCh38 chr5: 150,847,400-150,847,472 , GRCh37.p13 chr5: 150,226,962-150,227,034 IRGM
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7053584inversion1nstd229human GRCh38 chr5: 144,534,922-150,861,041 , GRCh37.p13 chr5: 143,914,485-150,240,603 SMIM3, NAMPTP2, 102 more genes
    nsv7045608inversion1nstd229human GRCh38 chr5: 142,902,498-151,105,008 , GRCh37.p13 chr5: 142,282,063-150,484,569 FBXO38-DT, POU4F3, 126 more genes
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6792831copy number variation1nstd229human GRCh38 chr5: 150,869,703-150,875,733 , GRCh37.p13 chr5: 150,249,265-150,255,295 IRGM
    nsv6790288copy number variation1nstd229human GRCh38 chr5: 150,902,513-150,906,301 , GRCh37.p13 chr5: 150,282,075-150,285,863 ZNF300, IRGM
    nsv6789751copy number variation1nstd229human GRCh38 chr5: 150,883,459-150,883,486 , GRCh37.p13 chr5: 150,263,021-150,263,048 IRGM
    nsv6788740copy number variation1nstd229human GRCh38 chr5: 150,886,662-150,886,758 , GRCh37.p13 chr5: 150,266,224-150,266,320 IRGM
    nsv6787801copy number variation1nstd229human GRCh38 chr5: 150,871,712-150,878,794 , GRCh37.p13 chr5: 150,251,274-150,258,356 IRGM
    nsv6630547copy number variation1nstd224human GRCh37 chr5: 150,253,104-150,331,600 , GRCh38.p12 chr5: 150,873,542-150,952,038 ZNF300, ZNF300P1, 1 more genes
    nsv6630312copy number variation1nstd224human GRCh37 chr5: 150,167,118-150,282,735 , GRCh38.p12 chr5: 150,787,556-150,903,173 ZNF300, SMIM3, 1 more genes
    nsv6572718inversion1nstd223human GRCh38 chr5: 150,878,179-150,879,139 , GRCh37.p13 chr5: 150,257,741-150,258,701 IRGM
    nsv6572167inversion1nstd223human GRCh38 chr5: 150,877,904-150,878,968 , GRCh37.p13 chr5: 150,257,466-150,258,530 IRGM
    nsv6413340copy number variation1nstd223human GRCh38 chr5: 150,889,901-150,891,500 , GRCh37.p13 chr5: 150,269,463-150,271,062 ZNF300, IRGM
    nsv6411596copy number variation1nstd223human GRCh38 chr5: 150,835,601-150,851,700 , GRCh37.p13 chr5: 150,215,163-150,231,262 IRGM
    nsv6407534copy number variation1nstd223human GRCh38 chr5: 150,777,592-150,935,919 , GRCh37.p13 chr5: 150,157,154-150,315,481 SMIM3, ZNF300, 2 more genes
    nsv6406171copy number variation1nstd223human GRCh38 chr5: 150,827,001-150,873,100 , GRCh37.p13 chr5: 150,206,563-150,252,662 IRGM
    nsv6403544copy number variation1nstd223human GRCh38 chr5: 150,820,501-150,846,400 , GRCh37.p13 chr5: 150,200,063-150,225,962 IRGM
    nsv6400223copy number variation1nstd223human GRCh38 chr5: 150,902,513-150,906,298 , GRCh37.p13 chr5: 150,282,075-150,285,860 ZNF300, IRGM
    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