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 166

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6975585copy number variation1nstd229human GRCh38 chr15: 43,624,353-43,787,662 , GRCh37.p13 chr15: 43,916,551-44,079,860 RNU6-610P, ELL3, 11 more genes
    nsv6975170copy number variation1nstd229human GRCh38 chr15: 43,479,701-43,751,300 , GRCh37.p13 chr15: 43,771,899-44,043,498 CKMT1B, PPIP5K1P1-CATSPER2, 15 more genes
    nsv6623114copy number variation3nstd224human GRCh37 chr15: 43,924,420-44,038,850 , GRCh38.p12 chr15: 43,632,222-43,746,652 CKMT1A, STRCP1, 9 more genes
    nsv6506961copy number variation1nstd223human GRCh38 chr15: 43,734,662-43,735,950 , GRCh37.p13 chr15: 44,026,860-44,028,148 RNU6-354P, CATSPER2P1
    nsv6291560copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,215,243-44,632,384 , GRCh38.p12 chr15: 42,923,045-44,340,186 PPIP5K1P1-CATSPER2, STRCP1, 44 more genes
    nsv6290201copy number variation1nstd102humanPathogenic GRCh37 chr15: 43,851,199-44,038,820 , GRCh38.p12 chr15: 43,559,001-43,746,622 CATSPER2P1, CKMT1A, 13 more genes
    nsv6290131copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr15: 43,851,199-44,038,794 , GRCh38.p12 chr15: 43,559,001-43,746,596 STRCP1, CKMT1B, 13 more genes
    nsv5848601copy number variation1nstd209human GRCh38 chr15: 43,727,291-43,743,597 , GRCh37.p13 chr15: 44,019,489-44,035,795 RNU6-354P, CATSPER2P1
    nsv5644823insertion1nstd207human GRCh38 chr15: 43,739,806-43,739,806 , GRCh37.p13 chr15: 44,032,004-44,032,004 CATSPER2P1
    nsv5602723copy number variation1nstd207human GRCh38 chr15: 43,740,633-43,740,881 , GRCh37.p13 chr15: 44,032,831-44,033,079 CATSPER2P1
    nsv5599032copy number variation1nstd207human GRCh38 chr15: 43,742,861-43,743,133 , GRCh37.p13 chr15: 44,035,059-44,035,331 CATSPER2P1
    nsv5597957copy number variation1nstd207human GRCh38 chr15: 43,745,472-43,745,779 , GRCh37.p13 chr15: 44,037,670-44,037,977 CATSPER2P1, PDIA3
    nsv5596311copy number variation1nstd207human GRCh38 chr15: 43,739,797-43,740,112 , GRCh37.p13 chr15: 44,031,995-44,032,310 CATSPER2P1
    nsv5512663copy number variation1nstd206human GRCh38 chr15: 43,718,874-43,744,874 , GRCh37.p13 chr15: 44,011,072-44,037,072 RNU6-354P, PDIA3, 1 more genes
    nsv5511934copy number variation1nstd206human GRCh38 chr15: 43,742,477-43,743,031 , GRCh37.p13 chr15: 44,034,675-44,035,229 CATSPER2P1
    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
    nsv5380052translocation1nstd200human GRCh38 chr15: 43,624,401-43,624,401 , GRCh38 chr15: 43,740,766-43,740,766 , GRCh37.p13 chr15: 43,916,599-43,916,599 , GRCh37.p13 chr15: 44,032,964-44,032,964 CATSPER2P1
    nsv5146539mobile element insertion1nstd203human GRCh38 chr15: 43,745,593-43,745,600 , GRCh37.p13 chr15: 44,037,791-44,037,798 PDIA3, CATSPER2P1
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 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