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 114

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5668558inversion1nstd207human GRCh38 chr9: 10,002-32,696 , GRCh37.p13 chr9: 10,002-32,696 FAM138C, WASHC1, 3 more genes
    nsv5244312copy number variation1nstd204human GRCh38.p13 chr9: 32,301-32,600 , GRCh37.p13 chr9: 32,301-32,600 FAM138C
    nsv4832934copy number variation1nstd200human GRCh37 chr12: 147,803-149,790 , GRCh38.p12 chr9: 34,251-36,239 FAM138C
    nsv4829390copy number variation1nstd200human GRCh37 chr9: 11,147-117,851 , GRCh38.p12 chr9: 11,147-117,851 MIR1302-9, PGM5P3-AS1, 7 more genes
    nsv4684191copy number variation1nstd102humanPathogenic GRCh38 chr9: 1-190,938 , GRCh37.p13 chr9: 10,001-190,938 WASHC1, PGM5P3, 10 more genes
    nsv4680973copy number variation1nstd189human GRCh37.p13 chr9: 1-362,584 , GRCh38.p12 chr9: 10,001-362,584 FOXD4, ZNG1A, 13 more genes
    nsv4680803copy number variation1nstd189human GRCh37.p13 chr9: 1-455,575 , GRCh38.p12 chr9: 10,001-455,575 FOXD4, ZNG1A, 13 more genes
    nsv4680273copy number variation1nstd189human GRCh37.p13 chr9: 1-506,362 , GRCh38.p12 chr9: 10,001-506,362 FOXD4, KANK1, 18 more genes
    nsv4679901copy number variation1nstd189human GRCh37.p13 chr9: 1-382,945 , GRCh38.p12 chr9: 10,001-382,945 FOXD4, ZNG1A, 13 more genes
    nsv4679707copy number variation1nstd189human GRCh37.p13 chr9: 1-359,517 , GRCh38.p12 chr9: 10,001-359,517 FOXD4, ZNG1A, 13 more genes
    nsv4679702copy number variation1nstd189human GRCh37.p13 chr9: 1-386,048 , GRCh38.p12 chr9: 10,001-386,048 FOXD4, ZNG1A, 13 more genes
    nsv4679691copy number variation1nstd189human GRCh37.p13 chr9: 1-387,585 , GRCh38.p12 chr9: 10,001-387,585 FOXD4, ZNG1A, 13 more genes
    nsv4679606copy number variation1nstd189human GRCh37.p13 chr9: 1-344,725 , GRCh38.p12 chr9: 10,001-344,725 FOXD4, ZNG1A, 12 more genes
    nsv4679431copy number variation1nstd189human GRCh37.p13 chr9: 1-414,637 , GRCh38.p12 chr9: 10,001-414,637 FOXD4, ZNG1A, 13 more genes
    nsv4679049copy number variation1nstd189human GRCh37.p13 chr9: 1-337,876 , GRCh38.p12 chr9: 10,001-337,876 FOXD4, ZNG1A, 12 more genes
    nsv4678913copy number variation1nstd189human GRCh37.p13 chr9: 1-286,850 , GRCh38.p12 chr9: 10,001-286,850 FOXD4, ZNG1A, 12 more genes
    nsv4671378copy number variation1nstd186human GRCh37 chr9: 20,627-169,919 , GRCh38.p12 chr9: 20,627-169,919 PGM5P3-AS1, ZNG1A, 8 more genes
    nsv4661074copy number variation2nstd186human GRCh37 chr12: 147,081-151,800 , GRCh38.p12 chr9: 33,828-38,256 FAM138C
    nsv4643769copy number variation2nstd186human GRCh37 chr12: 147,081-151,800 , GRCh38.p12 chr9: 33,828-38,256 FAM138C
    nsv4640427copy number variation4nstd186human GRCh37 chr12: 145,800-155,000 , GRCh38.p12 chr9: 33,828-38,937 FAM138C
    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