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 3368

    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
    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
    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
    esv3832010copy number variation73estd219human GRCh37 chr3: 128,378,657-128,404,290 , GRCh38.p12 chr3: 128,659,814-128,685,447 POU5F1P6
    esv3862620copy number variation80estd219human GRCh37 chr11: 1,914,893-1,937,398 , GRCh38.p12 chr11: 1,893,663-1,916,168 LINC01150
    esv3821155copy number variation879estd219human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3827261copy number variation1244estd219human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3821019copy number variation3estd219human GRCh37 chr1: 162,284,034-162,297,145 , GRCh38.p12 chr1: 162,314,244-162,327,355 NOS1AP
    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
    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
    esv3853510copy number variation1096estd219human GRCh37 chr8: 39,310,276-39,322,581 , GRCh38.p12 chr8: 39,452,757-39,465,062 ADAM3A
    esv3833638copy number variation2212estd219human GRCh37 chr3: 192,875,179-192,885,555 , GRCh38.p12 chr3: 193,157,390-193,167,766 VEZF1P1
    esv3845277copy number variation795estd219human GRCh37 chr6: 72,862,591-72,874,663 , GRCh38.p12 chr6: 72,152,888-72,164,960 RIMS1
    esv3866371copy number variation2414estd219human GRCh37 chr12: 8,558,280-8,568,490 , GRCh38.p12 chr12: 8,405,684-8,415,894 OR7E140P
    esv3821788copy number variation1068estd219human GRCh37 chr1: 196,733,744-196,745,476 , GRCh38.p12 chr1: 196,764,614-196,776,346 CFHR3
    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