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 317

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5915802copy number variation1nstd209human GRCh38 chr9: 4,956,818-6,213,781 , GRCh37.p13 chr9: 4,956,818-6,213,781 , RLN1, 30 more genes
    nsv5914606copy number variation1nstd209human GRCh38 chr9: 5,233,642-5,244,664 , GRCh37.p13 chr9: 5,233,642-5,244,664 INSL4
    nsv5861649copy number variation1nstd209human GRCh38 chr9: 5,233,777-5,238,413 , GRCh37.p13 chr9: 5,233,777-5,238,413 INSL4
    nsv5854243copy number variation2nstd209human GRCh38 chr9: 5,233,677-5,235,013 , GRCh37.p13 chr9: 5,233,677-5,235,013 INSL4
    nsv5381785copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,854,435-6,937,677 , GRCh38.p12 chr9: 2,854,435-6,937,677 GLIS3-AS1, RFX3-DT, 70 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 ACTG1P14, DMAC1, 191 more genes
    nsv5381702copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,029,023-5,300,444 , GRCh38.p12 chr9: 2,029,023-5,300,444 MTND5P36, MTND2P36, 53 more genes
    nsv5380518translocation1nstd200human GRCh38 chr2: 91,996,405-91,996,405 , GRCh38 chr9: 5,231,296-5,231,296 , GRCh37.p13 chr2: 92,184,431-92,184,431 , GRCh37.p13 chr9: 5,231,296-5,231,296 INSL4
    nsv5314214copy number variation1nstd204human GRCh38.p13 chr9: 4,872,969-5,692,972 , GRCh37.p13 chr9: 4,872,969-5,692,972 , INSL4, 23 more genes
    nsv5304641copy number variation1nstd204human GRCh37.p13 chr9: 5,160,079-5,230,073 , GRCh38.p13 chr9: 5,160,079-5,230,073 INSL6, INSL4
    nsv4963082copy number variation1nstd200human GRCh38 chr9: 5,227,629-5,236,618 , GRCh37.p13 chr9: 5,227,629-5,236,618 INSL4
    nsv4823132copy number variation1nstd200human GRCh37 chr9: 5,233,642-5,244,665 , GRCh38.p12 chr9: 5,233,642-5,244,665 INSL4
    nsv4814596copy number variation1nstd200human GRCh37 chr9: 4,872,979-5,692,966 , GRCh38.p12 chr9: 4,872,979-5,692,966 , RLN2, 23 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 DOCK8-AS1, RN7SL25P, 186 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
    nsv4675650copy number variation1nstd102humanUncertain significance GRCh37 chr9: 4,613,939-6,144,065 , GRCh38.p12 chr9: 4,613,939-6,144,065 INSL6, RIC1, 39 more genes
    nsv4675646copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-14,103,730 , GRCh38.p12 chr9: 203,861-14,103,731 INSL4, LINC02851, 145 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
    nsv4675043copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-14,080,419 , GRCh38.p12 chr9: 203,861-14,080,420 MTND2P36, MTND5P36, 145 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