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 3111

    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
    esv3831763copy number variation1estd219human GRCh37 chr3: 115,835,552-115,884,255 , GRCh38.p12 chr3: 116,116,705-116,165,408 LSAMP
    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
    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
    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
    esv3865854copy number variation30estd219human GRCh37 chr11: 126,235,306-126,251,893 , GRCh38.p12 chr11: 126,365,411-126,381,998 ST3GAL4
    esv3874672copy number variation227estd219human GRCh37 chr15: 32,504,287-32,519,739 , GRCh38.p12 chr15: 32,212,086-32,227,538 LOC102724078
    esv3873211copy number variation1estd219human GRCh37 chr14: 62,235,132-62,250,953 , GRCh38.p12 chr14: 61,768,414-61,784,235 SNAPC1
    esv3851465copy number variation1169estd219human GRCh37 chr7: 133,785,003-133,798,330 , GRCh38.p12 chr7: 134,100,250-134,113,577
    esv3830293copy number variation263estd219human GRCh37 chr3: 53,026,796-53,039,244 , GRCh38.p12 chr3: 52,992,780-53,005,228 SFMBT1
    esv3864936copy number variation232estd219human GRCh37 chr11: 89,798,932-89,810,560 , GRCh38.p12 chr11: 90,065,764-90,077,392 TRIM49C
    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
    esv3867759copy number variation98estd219human GRCh37 chr12: 62,200,798-62,210,961 , GRCh38.p12 chr12: 61,807,017-61,817,180 TAFA2
    esv3833638copy number variation2212estd219human GRCh37 chr3: 192,875,179-192,885,555 , GRCh38.p12 chr3: 193,157,390-193,167,766 VEZF1P1
    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