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 310

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7068608inversion1nstd229human GRCh38 chr19: 44,955,982-44,955,998 , GRCh37.p13 chr19: 45,459,239-45,459,255 CLPTM1
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7066137inversion1nstd229human GRCh38 chr19: 43,668,049-45,225,177 , GRCh37.p13 chr19: 44,172,201-45,728,435 LOC107985306, LYPD5, 67 more genes
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    nsv7017140copy number variation1nstd229human GRCh38 chr19: 44,895,100-44,984,838 , GRCh37.p13 chr19: 45,398,357-45,488,096 APOC4-APOC2, APOC2, 6 more genes
    nsv7016074copy number variation1nstd229human GRCh38 chr19: 44,964,055-44,967,096 , GRCh37.p13 chr19: 45,467,312-45,470,353 CLPTM1
    nsv7010965copy number variation1nstd229human GRCh38 chr19: 44,981,230-44,984,939 , GRCh37.p13 chr19: 45,484,487-45,488,197 CLPTM1
    nsv7010489copy number variation1nstd229human GRCh38 chr19: 44,978,791-44,981,724 , GRCh37.p13 chr19: 45,482,048-45,484,981 CLPTM1
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7006941copy number variation1nstd229human GRCh38 chr19: 44,959,101-44,963,900 , GRCh37.p13 chr19: 45,462,358-45,467,157 CLPTM1
    nsv7005040copy number variation1nstd229human GRCh38 chr19: 44,969,901-44,971,100 , GRCh37.p13 chr19: 45,473,158-45,474,357 CLPTM1
    nsv6999525copy number variation1nstd229human GRCh38 chr19: 44,945,580-44,972,176 , GRCh37.p13 chr19: 45,448,837-45,475,433 APOC4, APOC2, 2 more genes
    nsv6596154inversion1nstd223human GRCh38 chr19: 44,978,257-44,978,890 , GRCh37.p13 chr19: 45,481,514-45,482,147 CLPTM1
    nsv6534059copy number variation1nstd223human GRCh38 chr19: 44,981,230-44,984,939 , GRCh37.p13 chr19: 45,484,487-45,488,197 CLPTM1
    nsv6528175copy number variation1nstd223human GRCh38 chr19: 44,971,001-44,972,500 , GRCh37.p13 chr19: 45,474,258-45,475,757 CLPTM1
    nsv6527628copy number variation1nstd223human GRCh38 chr19: 44,993,543-44,998,694 , GRCh37.p13 chr19: 45,496,801-45,501,952 CLPTM1
    nsv6525179copy number variation1nstd223human GRCh38 chr19: 44,956,665-44,958,301 , GRCh37.p13 chr19: 45,459,922-45,461,558 CLPTM1
    nsv6523815copy number variation1nstd223human GRCh38 chr19: 44,276,620-45,370,613 , GRCh37.p13 chr19: 44,780,773-45,873,871 APOE, CEACAM16, 48 more genes
    nsv6522847copy number variation1nstd223human GRCh38 chr19: 44,964,020-44,967,095 , GRCh37.p13 chr19: 45,467,277-45,470,352 CLPTM1
    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