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 376

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077246inversion1nstd229human GRCh38 chr15: 64,487,767-67,498,498 , GRCh37.p13 chr15: 64,779,966-67,790,836 LETM1P1, MIR4512, 74 more genes
    nsv7074515inversion1nstd229human GRCh38 chr15: 67,046,432-67,056,885 , GRCh37.p13 chr15: 67,338,770-67,349,223 SMAD3-DT
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7069168inversion1nstd229human GRCh38 chr15: 65,085,774-67,006,275 , GRCh37.p13 chr15: 65,378,112-67,298,613 MEGF11, HNRNPA1P44, 51 more genes
    nsv7064511inversion1nstd229human GRCh38 chr15: 67,051,781-67,056,735 , GRCh37.p13 chr15: 67,344,119-67,349,073 SMAD3-DT
    nsv6971925copy number variation1nstd229human GRCh38 chr15: 66,994,574-66,994,607 , GRCh37.p13 chr15: 67,286,912-67,286,945 SMAD3-DT
    nsv6970643copy number variation1nstd229human GRCh38 chr15: 66,985,201-67,031,200 , GRCh37.p13 chr15: 67,277,539-67,323,538 HMGN2P47, SMAD3-DT
    nsv6968886copy number variation1nstd229human GRCh38 chr15: 67,039,446-67,042,545 , GRCh37.p13 chr15: 67,331,784-67,334,883 SMAD3-DT
    nsv6968027copy number variation1nstd229human GRCh38 chr15: 67,002,865-67,005,325 , GRCh37.p13 chr15: 67,295,203-67,297,663 SMAD3-DT
    nsv6967429copy number variation1nstd229human GRCh38 chr15: 67,055,001-67,057,200 , GRCh37.p13 chr15: 67,347,339-67,349,538 SMAD3-DT
    nsv6967007copy number variation1nstd229human GRCh38 chr15: 67,024,101-67,026,500 , GRCh37.p13 chr15: 67,316,439-67,318,838 SMAD3-DT
    nsv6965235copy number variation1nstd229human GRCh38 chr15: 67,037,243-67,041,633 , GRCh37.p13 chr15: 67,329,581-67,333,971 SMAD3-DT
    nsv6962818copy number variation1nstd229human GRCh38 chr15: 67,044,701-67,175,700 , GRCh37.p13 chr15: 67,337,039-67,468,038 SMAD3-DT, SMAD3
    nsv6961160copy number variation1nstd229human GRCh38 chr15: 66,983,206-66,987,839 , GRCh37.p13 chr15: 67,275,544-67,280,177 SMAD3-DT
    nsv6959023copy number variation1nstd229human GRCh38 chr15: 66,984,757-66,987,484 , GRCh37.p13 chr15: 67,277,095-67,279,822 SMAD3-DT
    nsv6587449inversion1nstd223human GRCh38 chr15: 67,055,838-67,056,890 , GRCh37.p13 chr15: 67,348,176-67,349,228 SMAD3-DT
    nsv6586365inversion1nstd223human GRCh38 chr15: 67,004,603-67,005,111 , GRCh37.p13 chr15: 67,296,941-67,297,449 SMAD3-DT
    nsv6575824inversion1nstd223human GRCh38 chr15: 67,055,824-67,056,839 , GRCh37.p13 chr15: 67,348,162-67,349,177 SMAD3-DT
    nsv6509817copy number variation1nstd223human GRCh38 chr15: 67,063,601-67,066,300 , GRCh37.p13 chr15: 67,355,939-67,358,638 SMAD3-DT, SMAD3
    nsv6507905copy number variation1nstd223human GRCh38 chr15: 67,024,059-67,026,507 , GRCh37.p13 chr15: 67,316,397-67,318,845 SMAD3-DT
    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