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 3989

    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
    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
    esv3842790copy number variation95estd219human GRCh37 chr5: 155,566,445-155,591,598 , GRCh38.p12 chr5: 156,139,435-156,164,588 SGCD
    esv3821155copy number variation879estd219human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3856296copy number variation62estd219human GRCh37 chr9: 5,383,925-5,404,804 , GRCh38.p12 chr9: 5,383,925-5,404,804 PLGRKT
    esv3862224copy number variation147estd219human GRCh37 chr10: 122,769,702-122,787,504 , GRCh38.p12 chr10: 121,010,189-121,027,991 LOC105378521
    esv3852311copy number variation601estd219human GRCh37 chr8: 2,250,517-2,266,603 , GRCh38.p12 chr8|NT_187576.1: 485,727-501,813 LOC105377783
    esv3842791copy number variation93estd219human GRCh37 chr5: 155,577,187-155,591,410 , GRCh38.p12 chr5: 156,150,177-156,164,400 SGCD
    esv3835157copy number variation24estd219human GRCh37 chr4: 54,068,129-54,082,115 , GRCh38.p12 chr4: 53,201,962-53,215,948 SCFD2
    esv3872666copy number variation16estd219human GRCh37 chr14: 41,471,989-41,485,649 , GRCh38.p12 chr14: 41,002,784-41,016,444 LINC02315
    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
    esv3890498copy number variation1565estd219human GRCh37 chrX: 154,789,197-154,803,370 , GRCh38.p12 chrX: 155,559,536-155,573,709 TMLHE
    esv3820413copy number variation357estd219human GRCh37 chr1: 111,376,500-111,388,793 , GRCh38.p12 chr1: 110,833,878-110,846,171 NRBF2P3
    esv3824114copy number variation7estd219human GRCh37 chr2: 46,967,554-46,979,144 , GRCh38.p12 chr2: 46,740,415-46,752,005 SOCS5
    esv3826057copy number variation42estd219human GRCh37 chr2: 130,544,831-130,555,517 , GRCh38.p12 chr2: 129,787,258-129,797,944 LOC107985945
    esv3847132copy number variation2estd219human GRCh37 chr6: 147,323,438-147,335,051 , GRCh38.p12 chr6: 147,002,302-147,013,915 STXBP5-AS1
    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