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 3582

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3853507copy number variation1095estd219human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    esv3847578copy number variation4estd219human GRCh37 chr6: 162,999,037-163,054,047 , GRCh38.p12 chr6: 162,578,005-162,633,015 PRKN
    esv3849684copy number variation23estd219human GRCh37 chr7: 64,843,883-64,888,031 , GRCh38.p12 chr7: 65,378,970-65,423,118 ZNF92
    esv3847562copy number variation6estd219human GRCh37 chr6: 162,919,254-162,960,561 , GRCh38.p12 chr6: 162,498,222-162,539,529 PRKN
    esv3820750copy number variation2473estd219human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3846115copy number variation15estd219human GRCh37 chr6: 104,899,310-104,937,748 , GRCh38.p12 chr6: 104,451,435-104,489,873 LOC105377918
    esv3884482copy number variation2409estd219human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3835569copy number variation1672estd219human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3847564copy number variation7estd219human GRCh37 chr6: 162,924,604-162,946,412 , GRCh38.p12 chr6: 162,503,572-162,525,380 PRKN
    esv3821155copy number variation879estd219human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3849682copy number variation23estd219human GRCh37 chr7: 64,832,797-64,850,432 , GRCh38.p12 chr7: 65,367,884-65,385,519 ZNF92
    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
    esv3850618copy number variation797estd219human GRCh37 chr7: 100,327,251-100,341,280 , GRCh38.p12 chr7: 100,729,628-100,743,657 ZAN
    esv3890498copy number variation1565estd219human GRCh37 chrX: 154,789,197-154,803,370 , GRCh38.p12 chrX: 155,559,536-155,573,709 TMLHE
    esv3847566copy number variation6estd219human GRCh37 chr6: 162,949,194-162,959,850 , GRCh38.p12 chr6: 162,528,162-162,538,818 PRKN
    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
    esv3849666copy number variation4estd219human GRCh37 chr7: 64,681,079-64,691,382 , GRCh38.p12 chr7: 65,220,701-65,231,004 INTS4P1
    esv3845277copy number variation795estd219human GRCh37 chr6: 72,862,591-72,874,663 , GRCh38.p12 chr6: 72,152,888-72,164,960 RIMS1
    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