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 280

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144843insertion1nstd232human GRCh37.p13 chr11: 2,417,200-2,417,200 , GRCh38.p12 chr11: 2,395,970-2,395,970 CD81
    nsv7143102insertion1nstd232human GRCh37.p13 chr11: 2,400,682-2,400,682 , GRCh38.p12 chr11: 2,379,452-2,379,452 CD81
    nsv7140438insertion1nstd232human GRCh37.p13 chr11: 2,417,201-2,417,201 , GRCh38.p12 chr11: 2,395,971-2,395,971 CD81
    nsv7137436copy number variation1nstd232human GRCh37.p13 chr11: 2,417,943-2,418,031 , GRCh38.p12 chr11: 2,396,713-2,396,801 CD81, TSSC4
    nsv7137223copy number variation1nstd232human GRCh37.p13 chr11: 2,406,833-2,406,894 , GRCh38.p12 chr11: 2,385,603-2,385,664 CD81
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv7093761copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,278,740-2,906,719 , GRCh38.p12 chr11: 1,257,510-2,885,489 TOLLIP-DT, KRTAP5-6, 58 more genes
    nsv6902598copy number variation1nstd229human GRCh38 chr11: 2,383,305-2,389,207 , GRCh37.p13 chr11: 2,404,535-2,410,437 CD81
    nsv6902243copy number variation1nstd229human GRCh38 chr11: 2,323,266-2,387,977 , GRCh37.p13 chr11: 2,344,496-2,409,207 CD81, LOC105376520, 2 more genes
    nsv6899345copy number variation1nstd229human GRCh38 chr11: 2,386,473-2,487,577 , GRCh37.p13 chr11: 2,407,703-2,508,807 KCNQ1, TRPM5, 2 more genes
    nsv6898745copy number variation1nstd229human GRCh38 chr11: 2,379,081-2,379,173 , GRCh37.p13 chr11: 2,400,311-2,400,403 CD81
    nsv6885276copy number variation1nstd229human GRCh38 chr11: 1,136,035-3,145,463 , GRCh37.p13 chr11: 1,129,943-3,166,693 KRTAP5-1, MIR675, 69 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
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6447429copy number variation1nstd223human GRCh38 chr11: 2,396,261-2,410,524 , GRCh37.p13 chr11: 2,417,491-2,431,754 CD81, TRPM5, 1 more genes
    nsv6445062copy number variation1nstd223human GRCh38 chr11: 2,332,828-2,810,839 , GRCh37.p13 chr11: 2,354,058-2,832,069 RPL26P30, CD81, 7 more genes
    nsv6440079copy number variation1nstd223human GRCh38 chr11: 2,323,266-2,387,977 , GRCh37.p13 chr11: 2,344,496-2,409,207 RPL26P30, CD81, 2 more genes
    nsv6438165copy number variation1nstd223human GRCh38 chr11: 737,066-3,896,161 , GRCh37.p13 chr11: 737,066-3,917,391 RNU6-878P, CARS1-AS1, 123 more genes
    nsv6315544copy number variation1nstd102humanUncertain significance GRCh37 chr11: 2,314,240-2,915,570 , GRCh38.p12 chr11: 2,293,010-2,894,340 COX6CP18, SLC22A18AS, 14 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 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