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 2586

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3609657copy number variation667estd214human GRCh37 chr6: 78,892,808-79,053,430 , GRCh38.p12 chr6: 78,183,091-78,343,713 LOC105377865
    esv3609663copy number variation670estd214human GRCh37 chr6: 78,967,097-79,036,275 , GRCh38.p12 chr6: 78,257,380-78,326,558 LOC105377865
    esv3634197copy number variation646estd214human GRCh37 chr14: 41,607,767-41,669,648 , GRCh38.p12 chr14: 41,138,564-41,200,445 LINC02315
    esv3616948copy number variation1095estd214human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    esv3587491copy number variation2473estd214human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3644983copy number variation2409estd214human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3600875copy number variation1672estd214human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3623922copy number variation1739estd214human GRCh37 chr10: 81,474,561-81,502,396 , GRCh38.p12 chr10: 79,714,805-79,742,640 NUTM2B-AS1
    esv3632602copy number variation198estd214human GRCh37 chr13: 69,244,390-69,269,055 , GRCh38.p12 chr13: 68,670,258-68,694,923 RN7SL761P
    esv3591709copy number variation1476estd214human GRCh37 chr2: 98,136,216-98,156,567 , GRCh38.p12 chr2: 97,519,753-97,540,104 ANKRD36B
    esv3628470copy number variation4908estd214human GRCh37 chr12: 8,568,920-8,587,027 , GRCh38.p12 chr12: 8,416,324-8,434,431 OR7E148P
    esv3623140copy number variation1029estd214human GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441 ASAH2
    esv3593502copy number variation1244estd214human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3596214copy number variation90estd214human GRCh37 chr3: 56,610,335-56,626,937 , GRCh38.p12 chr3: 56,576,307-56,592,909 CCDC66
    esv3609614copy number variation648estd214human GRCh37 chr6: 77,437,459-77,453,275 , GRCh38.p12 chr6: 76,727,742-76,743,558 LOC105377861
    esv3596213copy number variation130estd214human GRCh37 chr3: 56,607,734-56,621,640 , GRCh38.p12 chr3: 56,573,706-56,587,612 CCDC66
    esv3614304copy number variation797estd214human GRCh37 chr7: 100,327,251-100,341,280 , GRCh38.p12 chr7: 100,729,628-100,743,657 ZAN
    esv3818053copy number variation289estd214human GRCh37 chrY: 9,640,466-9,653,590 , GRCh38.p12 chrY: 9,802,857-9,815,981 TTTY22
    esv3632413copy number variation92estd214human GRCh37 chr13: 64,224,633-64,237,603 , GRCh38.p12 chr13: 63,650,500-63,663,470 LOC105370236
    esv3634910copy number variation1922estd214human GRCh37 chr14: 74,011,083-74,024,007 , GRCh38.p12 chr14: 73,544,379-73,557,303 HEATR4
    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