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 3878

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3834770copy number variation743estd219human GRCh37 chr4: 34,781,317-34,849,886 , GRCh38.p12 chr4|NW_003315915.1: 272,024-340,593 , GRCh38.p12 chr4: 34,779,695-34,848,264 LOC105378262
    esv3834769copy number variation743estd219human GRCh37 chr4: 34,779,933-34,828,997 , GRCh38.p12 chr4|NW_003315915.1: 270,640-319,704 , GRCh38.p12 chr4: 34,778,311-34,827,375 LOC105378262
    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
    esv3857199copy number variation26estd219human GRCh37 chr9: 28,738,986-28,767,444 , GRCh38.p12 chr9: 28,738,988-28,767,446 LINGO2
    esv3849967copy number variation159estd219human GRCh37 chr7: 74,537,210-74,561,105 , GRCh38.p12 chr7: 75,121,409-75,145,298 GTF2IRD2B
    esv3854325copy number variation229estd219human GRCh37 chr8: 75,310,126-75,331,296 , GRCh38.p12 chr8: 74,397,891-74,419,061 GDAP1
    esv3856296copy number variation62estd219human GRCh37 chr9: 5,383,925-5,404,804 , GRCh38.p12 chr9: 5,383,925-5,404,804 PLGRKT
    esv3848557copy number variation3estd219human GRCh37 chr7: 17,553,361-17,571,295 , GRCh38.p12 chr7: 17,513,737-17,531,671 LINC02889
    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
    esv3831745copy number variation505estd219human GRCh37 chr3: 114,656,928-114,668,577 , GRCh38.p12 chr3: 114,938,081-114,949,730 ZBTB20
    esv3875633copy number variation144estd219human GRCh37 chr15: 76,335,203-76,348,180 , GRCh38.p12 chr15: 76,042,862-76,055,839 NRG4
    esv3827269copy number variation329estd219human GRCh37 chr2: 180,410,908-180,422,736 , GRCh38.p12 chr2: 179,546,181-179,558,009 ZNF385B
    esv3857200copy number variation28estd219human GRCh37 chr9: 28,739,563-28,751,257 , GRCh38.p12 chr9: 28,739,565-28,751,259 LINGO2
    esv3867376copy number variation22estd219human GRCh37 chr12: 45,272,972-45,283,878 , GRCh38.p12 chr12: 44,879,189-44,890,095 NELL2
    esv3847448copy number variation21estd219human GRCh37 chr6: 160,627,742-160,638,092 , GRCh38.p12 chr6: 160,206,710-160,217,060 SLC22A2
    esv3833638copy number variation2212estd219human GRCh37 chr3: 192,875,179-192,885,555 , GRCh38.p12 chr3: 193,157,390-193,167,766 VEZF1P1
    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