U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 153

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3884726copy number variation1nstd102humanPathogenic GRCh38 chr11: 112,088,857-112,094,980 , GRCh37 chr11: 111,959,581-111,965,704 SDHD
    nsv6309033copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,959,581-111,965,694 , GRCh38.p12 chr11: 112,088,857-112,094,970 SDHD
    nsv4452548copy number variation1nstd102humanPathogenic GRCh38 chr11: 112,093,691-112,095,868 , GRCh37 chr11: 111,964,415-111,966,592 SDHD
    nsv3871389copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,965,519-111,965,704 , GRCh38 chr11: 112,094,795-112,094,980 SDHD
    nsv3876242copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,965,523-111,965,700 , GRCh38 chr11: 112,094,799-112,094,976 SDHD
    nsv4682890copy number variation2nstd102humanPathogenic GRCh37 chr11: 111,965,519-111,965,694 , GRCh38.p12 chr11: 112,094,795-112,094,970 SDHD
    nsv1398573copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 111,965,980-111,966,081 , GRCh38 chr11: 112,095,256-112,095,357 SDHD
    nsv4681078copy number variation2nstd102humanUncertain significance GRCh37 chr11: 111,958,526-111,965,694 , GRCh38.p12 chr11: 112,087,802-112,094,970 SDHD
    nsv6907348copy number variation1nstd229human GRCh38 chr11: 112,089,601-112,092,700 , GRCh37.p13 chr11: 111,960,325-111,963,424 SDHD
    nsv4203715copy number variation1nstd166human GRCh37.p13 chr11: 111,965,831-111,966,327 , GRCh38.p12 chr11: 112,095,107-112,095,603 SDHD
    esv3155589copy number variation1estd209human GRCh37 chr11: 111,960,823-111,960,825 , GRCh38.p12 chr11: 112,090,099-112,090,101 SDHD
    esv3155590copy number variation1estd209human GRCh37 chr11: 111,961,062-111,961,063 , GRCh38.p12 chr11: 112,090,338-112,090,339 SDHD
    esv2316888copy number variation1estd194human NCBI36 chr11: 111,468,191-111,468,192 , GRCh37.p13 chr11: 111,962,981-111,962,982 , GRCh38.p12 chr11: 112,092,257-112,092,258 SDHD
    esv1503080copy number variation1estd22human NCBI36 chr11: 111,466,034-111,466,036 , GRCh37.p13 chr11: 111,960,824-111,960,826 , GRCh38.p12 chr11: 112,090,100-112,090,102 SDHD
    esv1733881copy number variation1estd22human NCBI36 chr11: 111,466,272-111,466,273 , GRCh37.p13 chr11: 111,961,062-111,961,063 , GRCh38.p12 chr11: 112,090,338-112,090,339 SDHD
    nsv5268729copy number variation1nstd204human GRCh38.p13 chr11: 112,092,519-112,094,823 , GRCh37.p13 chr11: 111,963,243-111,965,547 SDHD
    nsv975979copy number variation97nstd82eastern lowland gorilla, Cross River gorilla, western lowland gorilla, Denisova hominin, human, pygmy chimpanzee, Pan troglodytes ellioti, Pan troglodytes schweinfurthii, Pan troglodytes troglodytes, Pan troglodytes verus, Sumatran orangutan, Bornean orangutan NCBI36 chr11: 111,464,887-111,472,441 , GRCh37.p13 chr11: 111,959,677-111,967,231 , GRCh38.p12 chr11: 112,088,953-112,096,507 SDHD
    nsv4506665mobile element insertion1nstd166human GRCh37.p13 chr11: 111,963,328-111,963,328 , GRCh38.p12 chr11: 112,092,604-112,092,604 SDHD
    esv2896241insertion1estd209human GRCh37 chr11: 111,960,377-111,960,377 , GRCh38.p12 chr11: 112,089,653-112,089,653 SDHD
    esv2450949insertion1estd197human NCBI36 chr11: 111,465,587-111,465,587 , GRCh37.p13 chr11: 111,960,377-111,960,377 , GRCh38.p12 chr11: 112,089,653-112,089,653 SDHD
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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