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 3122

    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
    esv3596068copy number variation520estd214human GRCh37 chr3: 46,803,577-46,851,159 , GRCh38.p12 chr3: 46,762,087-46,809,669 PRSS44P
    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
    esv3632214copy number variation1037estd214human GRCh37 chr13: 57,752,516-57,781,577 , GRCh38.p12 chr13: 57,178,382-57,207,443 MTCO2P3
    esv3588471copy number variation1062estd214human GRCh37 chr1: 196,735,895-196,764,940 , GRCh38.p12 chr1: 196,766,765-196,795,810 CFHR3
    esv3623922copy number variation1739estd214human GRCh37 chr10: 81,474,561-81,502,396 , GRCh38.p12 chr10: 79,714,805-79,742,640 NUTM2B-AS1
    esv3620473copy number variation1254estd214human GRCh37 chr9: 43,580,844-43,606,160 , GRCh38.p12 chr9: 42,208,229-42,233,545 LOC112268036
    esv3603772copy number variation1611estd214human GRCh37 chr5: 757,676-778,933 , GRCh38.p12 chr5: 757,561-778,818 ZDHHC11B
    esv3615450copy number variation178estd214human GRCh37 chr7: 149,862,878-149,883,330 , GRCh38.p12 chr7: 150,165,789-150,186,241 ACTR3C
    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
    esv3593502copy number variation1244estd214human GRCh37 chr2: 180,064,283-180,083,019 , GRCh38.p12 chr2: 179,199,556-179,218,292 SESTD1
    esv3615872copy number variation601estd214human GRCh37 chr8: 2,250,517-2,266,603 , GRCh38.p12 chr8|NT_187576.1: 485,727-501,813 LOC105377783
    esv3620460copy number variation1877estd214human GRCh37 chr9: 41,971,191-41,985,717 , GRCh38.p12 chr9: 39,826,173-39,840,699 FGF7P3
    esv3615090copy number variation1169estd214human GRCh37 chr7: 133,785,003-133,798,330 , GRCh38.p12 chr7: 134,100,250-134,113,577
    esv3614304copy number variation797estd214human GRCh37 chr7: 100,327,251-100,341,280 , GRCh38.p12 chr7: 100,729,628-100,743,657 ZAN
    esv3617163copy number variation10estd214human GRCh37 chr8: 51,098,363-51,111,470 , GRCh38.p12 chr8: 50,185,803-50,198,910 SNTG1
    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