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 159

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076610inversion1nstd229human GRCh38 chr11: 8,997,198-8,998,829 , GRCh37.p13 chr11: 9,018,745-9,020,376 NRIP3
    nsv7075059inversion1nstd229human GRCh38 chr11: 8,975,494-9,151,033 , GRCh37.p13 chr11: 8,997,041-9,172,580 DENND5A, MIR5691, 6 more genes
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 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
    nsv6909430copy number variation1nstd229human GRCh38 chr11: 8,911,101-8,979,500 , GRCh37.p13 chr11: 8,932,648-9,001,047 C11orf16, ASCL3, 5 more genes
    nsv6907390copy number variation1nstd229human GRCh38 chr11: 9,001,722-9,001,880 , GRCh37.p13 chr11: 9,023,269-9,023,427 NRIP3
    nsv6906971copy number variation1nstd229human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 RIC3, LOC644656, 86 more genes
    nsv6901413copy number variation1nstd229human GRCh38 chr11: 8,992,776-8,993,683 , GRCh37.p13 chr11: 9,014,323-9,015,230 NRIP3
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6454479copy number variation1nstd223human GRCh38 chr11: 8,986,856-8,991,136 , GRCh37.p13 chr11: 9,008,403-9,012,683 NRIP3
    nsv6453605copy number variation1nstd223human GRCh38 chr11: 8,836,740-9,205,220 , GRCh37.p13 chr11: 8,858,287-9,226,767 MIR5691, LOC105376542, 12 more genes
    nsv6442904copy number variation1nstd223human GRCh38 chr11: 9,001,722-9,001,880 , GRCh37.p13 chr11: 9,023,269-9,023,427 NRIP3
    nsv6442855copy number variation1nstd223human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 LOC105369149, C11orf16, 86 more genes
    nsv6441020copy number variation1nstd223human GRCh38 chr11: 8,965,667-8,985,445 , GRCh37.p13 chr11: 8,987,214-9,006,992 TMEM9B-AS1, NRIP3
    nsv6439021copy number variation1nstd223human GRCh38 chr11: 9,000,050-9,040,655 , GRCh37.p13 chr11: 9,021,597-9,062,202 NRIP3-DT, NRIP3, 1 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
    nsv6094420insertion1nstd212human GRCh38 chr11: 8,978,838-8,978,838 , GRCh37.p13 chr11: 9,000,385-9,000,385 NRIP3
    nsv6032363copy number variation1nstd212human GRCh38 chr11: 8,978,633-8,978,745 , GRCh37.p13 chr11: 9,000,180-9,000,292 NRIP3
    nsv6031495copy number variation1nstd212human GRCh38 chr11: 8,978,675-8,978,902 , GRCh37.p13 chr11: 9,000,222-9,000,449 NRIP3
    nsv6030464copy number variation1nstd212human GRCh37.p13 chr11: 8,839,646-9,001,117 , GRCh38 chr11: 8,818,099-8,979,570 DENND2B, AKIP1, 6 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