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 4016

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3830173copy number variation520estd219human GRCh37 chr3: 46,803,577-46,851,159 , GRCh38.p12 chr3: 46,762,087-46,809,669 PRSS44P
    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
    esv3888081copy number variation6estd219human GRCh37 chrX: 2,365,748-2,400,662 , GRCh38.p12 chrX: 2,447,707-2,482,621 DHRSX
    esv3889359copy number variation26estd219human GRCh37 chrX: 80,748,583-80,780,550 , GRCh38.p12 chrX: 81,493,084-81,525,051 LOC105373285
    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
    esv3849967copy number variation159estd219human GRCh37 chr7: 74,537,210-74,561,105 , GRCh38.p12 chr7: 75,121,409-75,145,298 GTF2IRD2B
    esv3876006copy number variation1estd219human GRCh37 chr15: 92,587,606-92,608,197 , GRCh38.p12 chr15: 92,044,376-92,064,967 SLCO3A1
    esv3854325copy number variation229estd219human GRCh37 chr8: 75,310,126-75,331,296 , GRCh38.p12 chr8: 74,397,891-74,419,061 GDAP1
    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
    esv3861771copy number variation716estd219human GRCh37 chr10: 100,688,139-100,702,531 , GRCh38.p12 chr10: 98,928,382-98,942,774 HPSE2
    esv3878137copy number variation1122estd219human GRCh37 chr16: 78,371,328-78,385,326 , GRCh38.p12 chr16: 78,337,431-78,351,429 WWOX
    esv3856804copy number variation37estd219human GRCh37 chr9: 17,256,478-17,269,907 , GRCh38.p12 chr9: 17,256,480-17,269,909 CNTLN
    esv3890498copy number variation1565estd219human GRCh37 chrX: 154,789,197-154,803,370 , GRCh38.p12 chrX: 155,559,536-155,573,709 TMLHE
    esv3832158copy number variation15estd219human GRCh37 chr3: 133,014,921-133,028,615 , GRCh38.p12 chr3: 133,296,077-133,309,771 TMEM108
    esv3875633copy number variation144estd219human GRCh37 chr15: 76,335,203-76,348,180 , GRCh38.p12 chr15: 76,042,862-76,055,839 NRG4
    esv3848096copy number variation146estd219human GRCh37 chr7: 6,129,998-6,141,944 , GRCh38.p12 chr7: 6,090,367-6,102,313 USP42
    esv3832889copy number variation8estd219human GRCh37 chr3: 164,300,990-164,313,109 , GRCh38.p12 chr3: 164,583,202-164,595,321 LOC105374191
    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