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 132

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094111copy number variation1nstd102humanPathogenic GRCh37 chr11: 85,339,652-86,666,127 , GRCh38.p12 chr11: 85,628,608-86,955,085 PRSS23, OR7E13P, 30 more genes
    nsv7093948copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,339,652-85,367,545 , GRCh38.p12 chr11: 85,628,608-85,656,501 CREBZF, TMEM126B, 2 more genes
    nsv7068892inversion1nstd229human GRCh38 chr11: 85,482,651-87,653,297 , GRCh37.p13 chr11: 85,193,695-87,364,189 , RNU6-1292P, 42 more genes
    nsv7062534inversion1nstd229human GRCh38 chr11: 83,132,580-86,771,462 , GRCh37.p13 chr11: 82,843,622-86,482,504 CCDC83, LOC100421303, 44 more genes
    nsv6914106copy number variation1nstd229human GRCh38 chr11: 85,494,651-85,925,994 , GRCh37.p13 chr11: 85,205,695-85,637,037 SYTL2, CREBZF, 7 more genes
    nsv6905543copy number variation1nstd229human GRCh38 chr11: 84,763,504-86,648,143 , GRCh37.p13 chr11: 84,474,547-86,359,185 CCDC83, CCDC81, 25 more genes
    nsv6902416copy number variation1nstd229human GRCh38 chr11: 85,286,883-85,726,573 , GRCh37.p13 chr11: 84,997,927-85,437,616 RNU6-1292P, LOC100419092, 7 more genes
    nsv6901239copy number variation1nstd229human GRCh38 chr11: 85,654,490-85,732,964 , GRCh37.p13 chr11: 85,365,534-85,444,007 CCDC89, TMEM126A, 2 more genes
    nsv6637847copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899 PRSS23, MTCO3P25, 92 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6584412inversion1nstd223human GRCh38 chr11: 85,506,446-86,544,042 , GRCh37.p13 chr11: 85,217,490-86,255,084 RNU6-1292P, CCDC81, 22 more genes
    nsv6462238copy number variation1nstd223human GRCh38 chr11: 84,663,295-85,663,452 , GRCh37.p13 chr11: 84,374,338-85,374,496 TMEM126B, TMEM126A, 6 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6132193copy number variation1nstd213human GRCh37 chr11: 84,740,000-86,080,001 , GRCh38.p12 chr11: 85,028,956-86,368,959 TMEM126B, LOC100289518, 21 more genes
    nsv5920899copy number variation1nstd209human GRCh38 chr11: 85,426,274-86,526,514 , GRCh37.p13 chr11: 85,137,318-86,237,556 SYTL2, ME3, 23 more genes
    nsv5855276copy number variation1nstd209human GRCh38 chr11: 85,654,999-85,657,848 , GRCh37.p13 chr11: 85,366,043-85,368,892 CREBZF, TMEM126A
    nsv5701065mobile element insertion1nstd211human GRCh38 chr11: 85,647,134-85,647,134 , GRCh37.p13 chr11: 85,358,178-85,358,178 TMEM126A
    nsv5494209copy number variation1nstd206human GRCh38 chr11: 85,645,930-85,652,750 , GRCh37.p13 chr11: 85,356,974-85,363,794 TMEM126A
    nsv5412051mobile element insertion1nstd206human GRCh38 chr11: 85,647,134-85,647,185 , GRCh37.p13 chr11: 85,358,178-85,358,229 TMEM126A
    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