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 109

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939106copy number variation1nstd209human GRCh38 chr15: 38,008,106-40,186,655 , GRCh37.p13 chr15: 38,300,307-40,478,856 , LOC105370784, 36 more genes
    nsv5506609copy number variation1nstd206human GRCh38 chr15: 39,250,489-39,250,558 , GRCh37.p13 chr15: 39,542,690-39,542,759 LINC02915
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv4855793copy number variation1nstd200human GRCh37 chr15: 34,109,797-39,904,401 , GRCh38.p12 chr15: 33,817,596-39,612,200 , AQR, 87 more genes
    nsv4729292copy number variation1nstd102humanUncertain significance GRCh37 chr15: 38,632,117-39,790,989 , GRCh38.p12 chr15: 38,339,916-39,498,788 LOC102724253, FAM98B, 12 more genes
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv4249258copy number variation1nstd166human GRCh37.p13 chr15: 39,546,966-39,547,026 , GRCh38.p12 chr15: 39,254,765-39,254,825 LINC02915
    nsv4245248copy number variation1nstd166human GRCh37.p13 chr15: 39,005,375-39,583,447 , GRCh38.p12 chr15: 38,713,174-39,291,246 LINC02915, LOC102724253, 4 more genes
    nsv4242708copy number variation1nstd166human GRCh37.p13 chr15: 39,541,209-39,545,142 , GRCh38.p12 chr15: 39,249,008-39,252,941 LINC02915
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3920384copy number variation1nstd102humanPathogenic NCBI36 chr15: 30,405,629-37,473,561 , GRCh38 chr15: 32,326,136-39,394,068 , GRCh37 chr15: 32,618,337-39,686,269 PGBD4, LOC105370763, 113 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3919055copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,880,216-39,572,605 , NCBI36 chr15: 32,667,508-37,359,897 , GRCh38 chr15: 34,588,015-39,280,404 DPH6, NUTF2P6, 56 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917628copy number variation1nstd102humanUncertain significance NCBI36 chr15: 37,318,054-37,453,780 , GRCh37.p13 chr15: 39,530,762-39,666,488 , GRCh38.p12 chr15: 39,238,561-39,374,287 LINC02915
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3915967copy number variation1nstd102humanPathogenic GRCh38 chr15: 32,635,803-40,233,825 , GRCh37 chr15: 32,928,004-40,526,026 , NCBI36 chr15: 30,715,296-38,313,318 ANP32AP1, FMN1, 112 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 RPL21P113, LOC112268152, 1428 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 MIR4513, LOC727751, 1754 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