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 3436

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3875848copy number variation139estd219human GRCh37 chr15: 86,064,810-86,182,627 , GRCh38.p12 chr15: 85,521,579-85,639,396 AKAP13
    esv3872670copy number variation646estd219human GRCh37 chr14: 41,607,767-41,669,648 , GRCh38.p12 chr14: 41,138,564-41,200,445 LINC02315
    esv3853507copy number variation1095estd219human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    esv3820750copy number variation2473estd219human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3827689copy number variation1estd219human GRCh37 chr2: 196,991,074-197,025,868 , GRCh38.p12 chr2: 196,126,350-196,161,144 STK17B
    esv3884482copy number variation2409estd219human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3821789copy number variation1062estd219human GRCh37 chr1: 196,735,895-196,764,940 , GRCh38.p12 chr1: 196,766,765-196,795,810 CFHR3
    esv3835569copy number variation1672estd219human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3856453copy number variation2estd219human GRCh37 chr9: 9,685,887-9,709,990 , GRCh38.p12 chr9: 9,685,887-9,709,990 PTPRD
    esv3856454copy number variation3estd219human GRCh37 chr9: 9,685,868-9,708,326 , GRCh38.p12 chr9: 9,685,868-9,708,326 PTPRD
    esv3882282copy number variation6estd219human GRCh37 chr18: 67,079,359-67,096,206 , GRCh38.p12 chr18: 69,412,123-69,428,970 DOK6
    esv3874672copy number variation227estd219human GRCh37 chr15: 32,504,287-32,519,739 , GRCh38.p12 chr15: 32,212,086-32,227,538 LOC102724078
    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
    esv3858600copy number variation527estd219human GRCh37 chr9: 113,024,583-113,037,085 , GRCh38.p12 chr9: 110,262,303-110,274,805 LOC107987114
    esv3890498copy number variation1565estd219human GRCh37 chrX: 154,789,197-154,803,370 , GRCh38.p12 chrX: 155,559,536-155,573,709 TMLHE
    esv3831745copy number variation505estd219human GRCh37 chr3: 114,656,928-114,668,577 , GRCh38.p12 chr3: 114,938,081-114,949,730 ZBTB20
    esv3889030copy number variation80estd219human GRCh37 chrX: 61,988,565-62,000,220 , GRCh38.p12 chrX: 62,769,095-62,780,750 SSBL2P
    esv3865462copy number variation1142estd219human GRCh37 chr11: 107,234,989-107,247,884 , GRCh38.p12 chr11: 107,364,263-107,377,158 CWF19L2
    esv3858081copy number variation135estd219human GRCh37 chr9: 90,731,753-90,743,330 , GRCh38.p12 chr9: 88,116,838-88,128,415 SPATA31C2
    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