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 833

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097681copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,006,437-113,563,268 , GRCh38.p12 chr9: 110,244,157-110,800,988 LOC107987114, RPS21P5, 7 more genes
    nsv7068426inversion1nstd229human GRCh38 chr9: 110,371,716-110,395,003 , GRCh37.p13 chr9: 113,133,996-113,157,283 SVEP1
    nsv6876358copy number variation1nstd229human GRCh38 chr9: 110,385,928-110,386,064 , GRCh37.p13 chr9: 113,148,208-113,148,344 SVEP1
    nsv6876312copy number variation1nstd229human GRCh38 chr9: 110,576,920-110,583,297 , GRCh37.p13 chr9: 113,339,200-113,345,577 SVEP1
    nsv6875288copy number variation1nstd229human GRCh38 chr9: 110,562,187-110,562,402 , GRCh37.p13 chr9: 113,324,467-113,324,682 SVEP1
    nsv6875133copy number variation1nstd229human GRCh38 chr9: 110,562,359-110,567,581 , GRCh37.p13 chr9: 113,324,639-113,329,861 SVEP1
    nsv6872425copy number variation1nstd229human GRCh38 chr9: 110,560,811-110,566,563 , GRCh37.p13 chr9: 113,323,091-113,328,843 SVEP1
    nsv6869624copy number variation1nstd229human GRCh38 chr9: 110,388,517-110,388,575 , GRCh37.p13 chr9: 113,150,797-113,150,855 SVEP1
    nsv6866069copy number variation1nstd229human GRCh38 chr9: 110,448,001-110,456,000 , GRCh37.p13 chr9: 113,210,281-113,218,280 SVEP1
    nsv6866019copy number variation1nstd229human GRCh38 chr9: 110,502,906-110,503,042 , GRCh37.p13 chr9: 113,265,186-113,265,322 SVEP1
    nsv6865859copy number variation1nstd229human GRCh38 chr9: 110,375,809-110,375,873 , GRCh37.p13 chr9: 113,138,089-113,138,153 SVEP1
    nsv6865816copy number variation1nstd229human GRCh38 chr9: 110,384,576-110,384,611 , GRCh37.p13 chr9: 113,146,856-113,146,891 SVEP1
    nsv6864918copy number variation1nstd229human GRCh38 chr9: 110,477,532-110,479,149 , GRCh37.p13 chr9: 113,239,812-113,241,429 SVEP1
    nsv6864531copy number variation1nstd229human GRCh38 chr9: 110,525,887-110,535,535 , GRCh37.p13 chr9: 113,288,167-113,297,815 SVEP1
    nsv6864307copy number variation1nstd229human GRCh38 chr9: 110,538,485-110,538,856 , GRCh37.p13 chr9: 113,300,765-113,301,136 SVEP1
    nsv6863142copy number variation1nstd229human GRCh38 chr9: 110,516,851-110,528,992 , GRCh37.p13 chr9: 113,279,131-113,291,272 SVEP1
    nsv6860812copy number variation1nstd229human GRCh38 chr9: 110,383,823-110,383,854 , GRCh37.p13 chr9: 113,146,103-113,146,134 SVEP1
    nsv6859737copy number variation1nstd229human GRCh38 chr9: 110,499,486-110,504,062 , GRCh37.p13 chr9: 113,261,766-113,266,342 SVEP1
    nsv6858946copy number variation1nstd229human GRCh38 chr9: 110,444,188-110,444,720 , GRCh37.p13 chr9: 113,206,468-113,207,000 SVEP1
    nsv6858667copy number variation1nstd229human GRCh38 chr9: 110,337,501-110,395,000 , GRCh37.p13 chr9: 113,099,781-113,157,280 SVEP1, RNU6-1039P, 1 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