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 3221

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3856598copy number variation48estd219human GRCh37 chr9: 11,934,533-12,112,794 , GRCh38.p12 chr9: 11,934,533-12,112,794 LOC105375976
    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
    esv3827609copy number variation31estd219human GRCh37 chr2: 194,578,564-194,613,101 , GRCh38.p12 chr2: 193,713,840-193,748,377 SEC61GP1
    esv3835569copy number variation1672estd219human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3841841copy number variation1estd219human GRCh37 chr5: 117,534,298-117,557,331 , GRCh38.p12 chr5: 118,198,603-118,221,636 LINC02147
    esv3827608copy number variation40estd219human GRCh37 chr2: 194,577,966-194,601,084 , GRCh38.p12 chr2: 193,713,242-193,736,360 SEC61GP1
    esv3860443copy number variation1029estd219human GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441 ASAH2
    esv3879060copy number variation208estd219human GRCh37 chr17: 15,042,705-15,059,719 , GRCh38.p12 chr17: 15,139,388-15,156,402 LOC107984976
    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
    esv3841449copy number variation18estd219human GRCh37 chr5: 103,440,067-103,454,798 , GRCh38.p12 chr5: 104,104,366-104,119,097 NIHCOLE
    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
    esv3864936copy number variation232estd219human GRCh37 chr11: 89,798,932-89,810,560 , GRCh38.p12 chr11: 90,065,764-90,077,392 TRIM49C
    esv3865462copy number variation1142estd219human GRCh37 chr11: 107,234,989-107,247,884 , GRCh38.p12 chr11: 107,364,263-107,377,158 CWF19L2
    esv3818347copy number variation293estd219human GRCh37 chr1: 9,845,036-9,857,679 , GRCh38.p12 chr1: 9,784,978-9,797,621 CLSTN1
    esv3818888copy number variation539estd219human GRCh37 chr1: 35,101,427-35,111,985 , GRCh38.p12 chr1: 34,635,826-34,646,384 LOC105378641
    esv3853510copy number variation1096estd219human GRCh37 chr8: 39,310,276-39,322,581 , GRCh38.p12 chr8: 39,452,757-39,465,062 ADAM3A
    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