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 4004

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3820750copy number variation2473estd219human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3884482copy number variation2409estd219human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3870498copy number variation1037estd219human GRCh37 chr13: 57,752,516-57,781,577 , GRCh38.p12 chr13: 57,178,382-57,207,443 MTCO2P3
    esv3821789copy number variation1062estd219human GRCh37 chr1: 196,735,895-196,764,940 , GRCh38.p12 chr1: 196,766,765-196,795,810 CFHR3
    esv3862224copy number variation147estd219human GRCh37 chr10: 122,769,702-122,787,504 , GRCh38.p12 chr10: 121,010,189-121,027,991 LOC105378521
    esv3860443copy number variation1029estd219human GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441 ASAH2
    esv3827261copy number variation1244estd219human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3852311copy number variation601estd219human GRCh37 chr8: 2,250,517-2,266,603 , GRCh38.p12 chr8|NT_187576.1: 485,727-501,813 LOC105377783
    esv3827949copy number variation23estd219human GRCh37 chr2: 209,232,440-209,248,986 , GRCh38.p12 chr2: 208,367,715-208,384,261 PTH2R
    esv3831107copy number variation45estd219human GRCh37 chr3: 87,887,973-87,904,491 , GRCh38.p12 chr3: 87,838,823-87,855,341 HTR1F
    esv3819859copy number variation1estd219human GRCh37 chr1: 83,105,684-83,120,544 , GRCh38.p12 chr1: 82,640,001-82,654,861 LOC105378814
    esv3861771copy number variation716estd219human GRCh37 chr10: 100,688,139-100,702,531 , GRCh38.p12 chr10: 98,928,382-98,942,774 HPSE2
    esv3851465copy number variation1169estd219human GRCh37 chr7: 133,785,003-133,798,330 , GRCh38.p12 chr7: 134,100,250-134,113,577
    esv3878137copy number variation1122estd219human GRCh37 chr16: 78,371,328-78,385,326 , GRCh38.p12 chr16: 78,337,431-78,351,429 WWOX
    esv3827269copy number variation329estd219human GRCh37 chr2: 180,410,908-180,422,736 , GRCh38.p12 chr2: 179,546,181-179,558,009 ZNF385B
    esv3875416copy number variation17estd219human GRCh37 chr15: 64,996,598-65,008,762 , GRCh38.p12 chr15: 64,704,399-64,716,563
    esv3833638copy number variation2212estd219human GRCh37 chr3: 192,875,179-192,885,555 , GRCh38.p12 chr3: 193,157,390-193,167,766 VEZF1P1
    esv3833118copy number variation61estd219human GRCh37 chr3: 173,207,388-173,218,361 , GRCh38.p12 chr3: 173,489,598-173,500,571 NLGN1
    esv3866371copy number variation2414estd219human GRCh37 chr12: 8,558,280-8,568,490 , GRCh38.p12 chr12: 8,405,684-8,415,894 OR7E140P
    esv3821788copy number variation1068estd219human GRCh37 chr1: 196,733,744-196,745,476 , GRCh38.p12 chr1: 196,764,614-196,776,346 CFHR3
    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