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 246

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093698copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,411,829-6,662,844 , GRCh38.p12 chr11: 6,390,599-6,641,613 SMPD1, HPX, 11 more genes
    nsv7077146inversion1nstd229human GRCh38 chr11: 6,475,304-6,546,520 , GRCh37.p13 chr11: 6,496,534-6,567,750 LOC644169, ARFIP2, 3 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
    nsv6913673copy number variation1nstd229human GRCh38 chr11: 6,505,501-6,518,300 , GRCh37.p13 chr11: 6,526,731-6,539,530 RRP8, DNHD1
    nsv6913388copy number variation1nstd229human GRCh38 chr11: 6,543,296-6,543,327 , GRCh37.p13 chr11: 6,564,526-6,564,557 RRP8, DNHD1
    nsv6911957copy number variation1nstd229human GRCh38 chr11: 6,532,003-6,536,272 , GRCh37.p13 chr11: 6,553,233-6,557,502 RRP8, DNHD1
    nsv6911833copy number variation1nstd229human GRCh38 chr11: 6,548,584-6,552,718 , GRCh37.p13 chr11: 6,569,814-6,573,948 RRP8, DNHD1
    nsv6910934copy number variation1nstd229human GRCh38 chr11: 6,565,039-6,565,197 , GRCh37.p13 chr11: 6,586,269-6,586,427 RRP8, DNHD1
    nsv6910536copy number variation1nstd229human GRCh38 chr11: 6,494,527-6,501,861 , GRCh37.p13 chr11: 6,515,757-6,523,091 DNHD1
    nsv6908652copy number variation1nstd229human GRCh38 chr11: 6,545,295-6,546,860 , GRCh37.p13 chr11: 6,566,525-6,568,090 RRP8, DNHD1
    nsv6908165copy number variation1nstd229human GRCh38 chr11: 6,477,909-6,599,930 , GRCh37.p13 chr11: 6,499,139-6,621,160 LOC644169, ARFIP2, 3 more genes
    nsv6907424copy number variation1nstd229human GRCh38 chr11: 6,551,849-6,552,298 , GRCh37.p13 chr11: 6,573,079-6,573,528 RRP8, DNHD1
    nsv6905010copy number variation1nstd229human GRCh38 chr11: 6,509,446-6,509,640 , GRCh37.p13 chr11: 6,530,676-6,530,870 DNHD1
    nsv6903104copy number variation1nstd229human GRCh38 chr11: 6,545,701-6,661,700 , GRCh37.p13 chr11: 6,566,931-6,682,931 TPP1, DNHD1, 4 more genes
    nsv6900827copy number variation1nstd229human GRCh38 chr11: 6,191,411-6,542,996 , GRCh37.p13 chr11: 6,212,641-6,564,226 ARFIP2, RRP8, 14 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6589100inversion1nstd223human GRCh38 chr11: 6,507,241-6,508,360 , GRCh37.p13 chr11: 6,528,471-6,529,590 DNHD1
    nsv6577953inversion1nstd223human GRCh38 chr11: 6,517,541-6,517,658 , GRCh37.p13 chr11: 6,538,771-6,538,888 RRP8, DNHD1
    nsv6455363copy number variation1nstd223human GRCh38 chr11: 6,529,697-6,530,221 , GRCh37.p13 chr11: 6,550,927-6,551,451 RRP8, DNHD1
    nsv6455271copy number variation1nstd223human GRCh38 chr11: 6,532,003-6,536,269 , GRCh37.p13 chr11: 6,553,233-6,557,499 DNHD1, RRP8
    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