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 259

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140770insertion1nstd232human GRCh37.p13 chr11: 4,139,692-4,139,692 , GRCh38.p12 chr11: 4,118,462-4,118,462 RRM1
    nsv7137680copy number variation1nstd232human GRCh37.p13 chr11: 4,158,857-4,158,905 , GRCh38.p12 chr11: 4,137,627-4,137,675 RRM1
    nsv7067580inversion1nstd229human GRCh38 chr11: 4,132,046-4,493,992 , GRCh37.p13 chr11: 4,153,276-4,515,222 OR52K3P, SSU72L3, 16 more genes
    nsv7060920inversion1nstd229human GRCh38 chr11: 4,014,616-4,536,086 , GRCh37.p13 chr11: 4,035,846-4,557,316 RDXP1, RRM1, 19 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6916129copy number variation1nstd229human GRCh38 chr11: 3,833,721-4,728,036 , GRCh37.p13 chr11: 3,854,951-4,749,266 OR52K1, OR52B4, 39 more genes
    nsv6908511copy number variation1nstd229human GRCh38 chr11: 4,112,575-4,141,359 , GRCh37.p13 chr11: 4,133,805-4,162,589 RRM1
    nsv6905964copy number variation1nstd229human GRCh38 chr11: 4,120,301-4,128,600 , GRCh37.p13 chr11: 4,141,531-4,149,830 RRM1
    nsv6905533copy number variation1nstd229human GRCh38 chr11: 4,091,252-4,099,134 , GRCh37.p13 chr11: 4,112,482-4,120,364 STIM1, RRM1
    nsv6903369copy number variation1nstd229human GRCh38 chr11: 4,135,271-4,138,192 , GRCh37.p13 chr11: 4,156,501-4,159,422 RRM1
    nsv6901872copy number variation1nstd229human GRCh38 chr11: 4,095,390-4,095,418 , GRCh37.p13 chr11: 4,116,620-4,116,648 RRM1
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6621093copy number variation1nstd224human GRCh37 chr11: 4,112,732-4,234,786 , GRCh38.p12 chr11: 4,091,502-4,213,556 RDXP1, LINC02749, 3 more genes
    nsv6620748copy number variation1nstd224human GRCh37 chr11: 4,132,858-4,234,786 , GRCh38.p12 chr11: 4,111,628-4,213,556 RRM1, RDXP1, 2 more genes
    nsv6593981inversion1nstd223human GRCh38 chr11: 4,110,270-4,110,732 , GRCh37.p13 chr11: 4,131,500-4,131,962 RRM1
    nsv6589166inversion1nstd223human GRCh38 chr11: 4,114,276-4,114,959 , GRCh37.p13 chr11: 4,135,506-4,136,189 RRM1
    nsv6588280inversion1nstd223human GRCh38 chr11: 4,106,468-4,107,188 , GRCh37.p13 chr11: 4,127,698-4,128,418 RRM1
    nsv6580462inversion1nstd223human GRCh38 chr11: 4,101,316-4,102,404 , GRCh37.p13 chr11: 4,122,546-4,123,634 RRM1
    nsv6444361copy number variation1nstd223human GRCh38 chr11: 4,136,179-4,136,982 , GRCh37.p13 chr11: 4,157,409-4,158,212 RRM1
    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