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 4088

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3863259copy number variation4estd219human GRCh37 chr11: 25,129,111-25,315,252 , GRCh38.p12 chr11: 25,107,565-25,293,706 , GRCh38.p12 chr11|NW_003315936.1: 1-129,033 LOC100130747
    esv3863258copy number variation4estd219human GRCh37 chr11: 25,129,111-25,257,275 , GRCh38.p12 chr11: 25,107,565-25,235,729 , GRCh38.p12 chr11|NW_003315936.1: 1-71,056 LOC100130747
    esv3863262copy number variation4estd219human GRCh37 chr11: 25,144,555-25,216,073 , GRCh38.p12 chr11: 25,123,009-25,194,527 LOC100130747
    esv3848154copy number variation5estd219human GRCh37 chr7: 7,320,084-7,384,254 , GRCh38.p12 chr7: 7,280,453-7,344,623 COL28A1
    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
    esv3848975copy number variation54estd219human GRCh37 chr7: 34,895,675-34,913,807 , GRCh38.p12 chr7: 34,856,063-34,874,195 NPSR1
    esv3862224copy number variation147estd219human GRCh37 chr10: 122,769,702-122,787,504 , GRCh38.p12 chr10: 121,010,189-121,027,991 LOC105378521
    esv3847509copy number variation19estd219human GRCh37 chr6: 162,494,422-162,511,711 , GRCh38.p12 chr6: 162,073,390-162,090,679 PRKN
    esv3860443copy number variation1029estd219human GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441 ASAH2
    esv3827261copy number variation1244estd219human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3842791copy number variation93estd219human GRCh37 chr5: 155,577,187-155,591,410 , GRCh38.p12 chr5: 156,150,177-156,164,400 SGCD
    esv3861771copy number variation716estd219human GRCh37 chr10: 100,688,139-100,702,531 , GRCh38.p12 chr10: 98,928,382-98,942,774 HPSE2
    esv3831745copy number variation505estd219human GRCh37 chr3: 114,656,928-114,668,577 , GRCh38.p12 chr3: 114,938,081-114,949,730 ZBTB20
    esv3875633copy number variation144estd219human GRCh37 chr15: 76,335,203-76,348,180 , GRCh38.p12 chr15: 76,042,862-76,055,839 NRG4
    esv3827269copy number variation329estd219human GRCh37 chr2: 180,410,908-180,422,736 , GRCh38.p12 chr2: 179,546,181-179,558,009 ZNF385B
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center