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 241

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922438copy number variation1nstd209human GRCh38 chr9: 21,452,740-21,489,024 , GRCh37.p13 chr9: 21,452,739-21,489,023 IFNWP19, IFNE, 1 more genes
    nsv5914630copy number variation1nstd209human GRCh38 chr9: 21,479,211-21,486,761 , GRCh37.p13 chr9: 21,479,210-21,486,760 IFNE, MIR31HG
    nsv5861005copy number variation2nstd209human GRCh38 chr9: 21,475,277-21,486,003 , GRCh37.p13 chr9: 21,475,276-21,486,002 IFNE, MIR31HG
    nsv5854592copy number variation2nstd209human GRCh38 chr9: 21,479,101-21,486,603 , GRCh37.p13 chr9: 21,479,100-21,486,602 IFNE, MIR31HG
    nsv5590724copy number variation1nstd207human GRCh38 chr9: 21,481,022-21,492,252 , GRCh37.p13 chr9: 21,481,021-21,492,251 IFNE, MIR31HG
    nsv5491171copy number variation1nstd206human GRCh38 chr9: 21,481,025-21,492,253 , GRCh37.p13 chr9: 21,481,024-21,492,252 MIR31HG, IFNE
    nsv5488515copy number variation1nstd206human GRCh38 chr9: 21,481,098-21,483,263 , GRCh37.p13 chr9: 21,481,097-21,483,262 MIR31HG, IFNE
    nsv5482238copy number variation1nstd206human GRCh38 chr9: 21,479,211-21,486,765 , GRCh37.p13 chr9: 21,479,210-21,486,764 IFNE, MIR31HG
    nsv5479124copy number variation1nstd206human GRCh38 chr9: 21,447,873-21,480,507 , GRCh37.p13 chr9: 21,447,872-21,480,506 IFNE, IFNWP19, 1 more genes
    nsv4963641copy number variation1nstd200human GRCh38 chr9: 21,481,025-21,492,253 , GRCh37.p13 chr9: 21,481,024-21,492,252 IFNE, MIR31HG
    nsv4963640copy number variation1nstd200human GRCh38 chr9: 21,481,098-21,483,261 , GRCh37.p13 chr9: 21,481,097-21,483,260 IFNE, MIR31HG
    nsv4963637copy number variation1nstd200human GRCh38 chr9: 21,453,599-21,524,962 , GRCh37.p13 chr9: 21,453,598-21,524,961 IFNWP19, MIR31HG, 2 more genes
    nsv4954550copy number variation1nstd200human GRCh38 chr9: 21,133,080-21,557,413 , GRCh37.p13 chr9: 21,133,079-21,557,412 IFNWP15, IFNA12P, 27 more genes
    nsv4823857copy number variation1nstd200human GRCh37 chr9: 21,481,096-21,483,262 , GRCh38.p12 chr9: 21,481,097-21,483,263 MIR31HG, IFNE
    nsv4823856copy number variation1nstd200human GRCh37 chr9: 21,481,024-21,492,252 , GRCh38.p12 chr9: 21,481,025-21,492,253 MIR31HG, IFNE
    nsv4823852copy number variation1nstd200human GRCh37 chr9: 21,452,741-21,489,026 , GRCh38.p12 chr9: 21,452,742-21,489,027 IFNE, MIR31HG, 1 more genes
    nsv4814679copy number variation1nstd200human GRCh37 chr9: 21,479,210-21,486,764 , GRCh38.p12 chr9: 21,479,211-21,486,765 IFNE, MIR31HG
    nsv4814668copy number variation1nstd200human GRCh37 chr9: 21,133,079-21,557,412 , GRCh38.p12 chr9: 21,133,080-21,557,413 IFNA4, IFNA11P, 27 more genes
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 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