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 1371

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2665446copy number variation21estd199human GRCh37 chr14: 41,608,245-41,671,292 , GRCh38.p12 chr14: 41,139,042-41,202,089 LINC02315
    esv2678472copy number variation114estd199human GRCh37 chr14: 41,609,436-41,669,664 , GRCh38.p12 chr14: 41,140,233-41,200,461 LINC02315
    esv2658503copy number variation100estd199human GRCh37 chr6: 32,454,245-32,508,892 , GRCh38.p12 chr6: 32,486,468-32,541,115 HLA-DRB5
    esv2676879copy number variation198estd199human GRCh37 chr4: 34,779,980-34,829,038 , GRCh38.p12 chr4: 34,778,358-34,827,416 , GRCh38.p12 chr4|NW_003315915.1: 270,687-319,745 LOC105378262
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2665540copy number variation104estd199human GRCh37 chr22: 17,240,645-17,278,192 , GRCh38.p12 chr22: 16,759,755-16,797,302 XKR3
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    esv2661219copy number variation458estd199human GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103 SPIDR
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2672929copy number variation23estd199human GRCh37 chr16: 60,081,112-60,098,561 , GRCh38.p12 chr16: 60,047,208-60,064,657 LINC02141
    esv2661457copy number variation8estd199human GRCh37 chr7: 102,351,566-102,367,905 , GRCh38.p12 chr7: 102,711,119-102,727,458 RASA4DP
    esv2660711copy number variation25estd199human GRCh37 chr8: 56,376,731-56,392,656 , GRCh38.p12 chr8: 55,464,171-55,480,096 XKR4
    esv2674647copy number variation204estd199human GRCh37 chr8: 56,377,729-56,393,641 , GRCh38.p12 chr8: 55,465,169-55,481,081 XKR4
    esv2659901copy number variation6estd199human GRCh37 chr12: 122,634,656-122,650,525 , GRCh38.p12 chr12: 122,150,109-122,165,978 LRRC43
    esv2671576copy number variation156estd199human GRCh37 chr7: 100,326,645-100,341,192 , GRCh38.p12 chr7: 100,729,022-100,743,569 ZAN
    esv2661917copy number variation4estd199human GRCh37 chr14: 41,472,001-41,485,669 , GRCh38.p12 chr14: 41,002,796-41,016,464 LINC02315
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2656701copy number variation437estd199human GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001 WWOX
    esv2664165copy number variation220estd199human GRCh37 chr7: 100,327,572-100,340,716 , GRCh38.p12 chr7: 100,729,949-100,743,093 ZAN
    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