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 21

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096458copy number variation1nstd102humanUncertain significance GRCh37 chr3: 25,642,571-25,642,736 , GRCh38.p12 chr3: 25,601,080-25,601,245 TOP2B
    nsv3880680copy number variation1nstd102humanBenign GRCh37 chr3: 25,564,929-25,654,677 , GRCh38.p12 chr3: 25,523,438-25,613,186 TOP2B, RARB
    nsv7096563copy number variation1nstd102humanUncertain significance GRCh37 chr3: 25,611,229-25,662,327 , GRCh38.p12 chr3: 25,569,738-25,620,836 TOP2B, RARB
    nsv4682210copy number variation1nstd102humanUncertain significance GRCh37 chr3: 25,611,229-25,638,127 , GRCh38.p12 chr3: 25,569,738-25,596,636 TOP2B, RARB
    nsv7096562copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr3: 25,470,223-25,824,881 , GRCh38.p12 chr3: 25,428,732-25,783,390 TOP2B, RARB, 6 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 TOP2B, LOC102724104, 291 more genes
    nsv4452346copy number variation1nstd102humanPathogenic GRCh37 chr3: 19,064,852-26,448,689 , GRCh38.p12 chr3: 19,023,360-26,407,198 TOP2B, RPL15, 71 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 TOP2B, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 TOP2B, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 TOP2B, RPL23AP49, 2875 more genes
    nsv3905127copy number variation1nstd102humanPathogenic GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521 TOP2B, LINC02022, 540 more genes
    nsv3876280copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-37,459,464 , GRCh38.p12 chr3: 20,213-37,417,973 TOP2B, OXTR, 460 more genes
    nsv3892895copy number variation1nstd102humanPathogenic GRCh38 chr3: 52,266-37,148,076 , GRCh37 chr3: 93,949-37,189,567 , NCBI36 chr3: 68,949-37,164,571 TOP2B, RPL34P11, 452 more genes
    nsv3878718copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-36,710,181 , GRCh38.p12 chr3: 20,213-36,668,690 TOP2B, LRRC3B, 436 more genes
    nsv3875913copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-33,958,201 , GRCh38.p12 chr3: 20,213-33,916,709 TOP2B, RPS27P11, 424 more genes
    nsv3901059copy number variation1nstd102humanPathogenic GRCh37 chr3: 73,914-30,105,699 , GRCh38 chr3: 32,241-30,064,208 , NCBI36 chr3: 48,914-30,080,703 TOP2B, RPL32, 369 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 TOP2B, RNU6-243P, 382 more genes
    nsv3923656copy number variation1nstd102humanPathogenic GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034 TOP2B, RN7SL4P, 348 more genes
    nsv3888895copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 25,045,365-32,691,140 , GRCh38.p12 chr3: 25,003,874-32,649,648 TOP2B, RARB, 83 more genes
    nsv3889550copy number variation1nstd102humanUncertain significance GRCh37 chr3: 25,329,791-25,719,030 , GRCh38.p12 chr3: 25,288,300-25,677,539 TOP2B, RARB-AS1, 5 more genes
    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