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 181

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5699092mobile element insertion1nstd211human GRCh38 chr9: 33,470,801-33,470,801 , GRCh37.p13 chr9: 33,470,799-33,470,799 NOL6
    nsv5557339sequence alteration1nstd206human GRCh38 chr9: 33,412,268-33,823,627 , GRCh37.p13 chr9: 33,412,266-33,823,625 AQP3, PRSS3, 24 more genes
    nsv5552234insertion1nstd206human GRCh38 chr9: 33,470,941-33,470,989 , GRCh37.p13 chr9: 33,470,939-33,470,987 NOL6
    nsv5479102copy number variation1nstd206human GRCh38 chr9: 33,472,830-33,510,934 , GRCh37.p13 chr9: 33,472,828-33,510,932 SUGT1P1, LOC107987061, 2 more genes
    nsv5477187copy number variation1nstd206human GRCh38 chr9: 33,460,898-33,460,967 , GRCh37.p13 chr9: 33,460,896-33,460,965 NOL6
    nsv5381740copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,399,559-33,541,225 , GRCh38.p12 chr9: 32,399,561-33,541,227 SMU1, RNU4ATAC15P, 38 more genes
    nsv4954647copy number variation1nstd200human GRCh38 chr9: 33,457,929-33,485,990 , GRCh37.p13 chr9: 33,457,927-33,485,988 LOC107987061, NOL6, 1 more genes
    nsv4828192copy number variation1nstd200human GRCh37 chr9: 33,474,197-33,474,308 , GRCh38.p12 chr9: 33,474,199-33,474,310 LOC107987061, NOL6
    nsv4814738copy number variation1nstd200human GRCh37 chr9: 33,457,929-33,485,986 , GRCh38.p12 chr9: 33,457,931-33,485,988 MIR6851, NOL6, 1 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
    nsv4729230copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 32,192,406-38,311,776 , GRCh38.p12 chr9: 32,192,408-38,311,779 ACO1, ANXA2P2, 210 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4616661copy number variation1nstd183human GRCh37 chr9: 33,296,380-33,574,904 , GRCh38.p12 chr9: 33,296,382-33,574,906 AQP3, MIR6851, 11 more genes
    nsv4547357insertion1nstd166human GRCh37.p13 chr9: 33,470,936-33,470,936 , GRCh38.p12 chr9: 33,470,938-33,470,938 NOL6
    nsv4527085copy number variation1nstd166human GRCh37.p13 chr9: 33,474,343-33,475,182 , GRCh38.p12 chr9: 33,474,345-33,475,184 NOL6, LOC107987061
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457200copy number variation2nstd102humanPathogenic GRCh37 chr9: 203,861-67,986,965 , GRCh38.p12 chr9: 203,861-67,919,519 ACO1, RNU6-1073P, 846 more genes
    nsv4456028copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-38,472,979 , GRCh38.p12 chr9: 203,861-38,472,982 SNORA30B, LOC100419692, 559 more genes
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 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