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 3144

    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
    esv3872783copy number variation74estd219human GRCh37 chr14: 44,488,567-44,536,408 , GRCh38.p12 chr14: 44,019,364-44,067,205 LINC02307
    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
    esv3872784copy number variation80estd219human GRCh37 chr14: 44,500,538-44,532,608 , GRCh38.p12 chr14: 44,031,335-44,063,405 LINC02307
    esv3877198copy number variation52estd219human GRCh37 chr16: 29,556,778-29,578,806 , GRCh38.p12 chr16: 29,545,457-29,567,485 SMG1P2
    esv3860443copy number variation1029estd219human GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441 ASAH2
    esv3857970copy number variation27estd219human GRCh37 chr9: 85,372,352-85,388,303 , GRCh38.p12 chr9: 82,757,437-82,773,388 LOC107987087
    esv3874672copy number variation227estd219human GRCh37 chr15: 32,504,287-32,519,739 , GRCh38.p12 chr15: 32,212,086-32,227,538 LOC102724078
    esv3851465copy number variation1169estd219human GRCh37 chr7: 133,785,003-133,798,330 , GRCh38.p12 chr7: 134,100,250-134,113,577
    esv3858600copy number variation527estd219human GRCh37 chr9: 113,024,583-113,037,085 , GRCh38.p12 chr9: 110,262,303-110,274,805 LOC107987114
    esv3827250copy number variation35estd219human GRCh37 chr2: 179,516,178-179,529,263 , GRCh38.p12 chr2: 178,651,451-178,664,536 TTN
    esv3864936copy number variation232estd219human GRCh37 chr11: 89,798,932-89,810,560 , GRCh38.p12 chr11: 90,065,764-90,077,392 TRIM49C
    esv3850412copy number variation193estd219human GRCh37 chr7: 91,030,693-91,042,943 , GRCh38.p12 chr7: 91,401,378-91,413,628 LINC02932
    esv3842123copy number variation25estd219human GRCh37 chr5: 126,230,402-126,241,621 , GRCh38.p12 chr5: 126,894,710-126,905,929 MARCHF3
    esv3835172copy number variation14estd219human GRCh37 chr4: 54,592,328-54,603,344 , GRCh38.p12 chr4: 53,726,161-53,737,177 LOC100506444
    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
    esv3828568copy number variation96estd219human GRCh37 chr2: 233,214,083-233,224,358 , GRCh38.p12 chr2: 232,349,373-232,359,648 ECEL1P3
    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