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 1127

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2676068copy number variation152estd199human GRCh37 chr6: 32,454,245-32,511,792 , GRCh38.p12 chr6: 32,486,468-32,544,015 HLA-DRB5
    esv2664200copy number variation92estd199human GRCh37 chr4: 75,282,645-75,323,192 , GRCh38.p12 chr4: 74,416,928-74,457,475 AREG
    esv2660522copy number variation236estd199human GRCh37 chr1: 207,700,012-207,737,123 , GRCh38.p12 chr1: 207,526,667-207,563,778 CR1
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2666578copy number variation167estd199human GRCh37 chr17: 77,462,245-77,494,392 , GRCh38.p12 chr17: 79,466,163-79,498,310 RBFOX3
    esv2658850copy number variation59estd199human GRCh37 chr16: 55,794,745-55,822,692 , GRCh38.p12 chr16: 55,760,833-55,788,780 CES1P1
    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
    esv2670760copy number variation36estd199human GRCh37 chr7: 100,326,395-100,343,242 , GRCh38.p12 chr7: 100,728,772-100,745,619 ZAN
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    esv2664983copy number variation7estd199human GRCh37 chr5: 114,706,251-114,721,123 , GRCh38.p12 chr5: 115,370,554-115,385,426 LOC105379130
    esv2663734copy number variation40estd199human GRCh37 chr7: 5,936,562-5,951,173 , GRCh38.p12 chr7: 5,896,931-5,911,542 CCZ1
    esv2662537copy number variation71estd199human GRCh37 chr3: 75,567,345-75,581,692 , GRCh38.p12 chr3: 75,518,194-75,532,541 SNRPCP10
    esv2663062copy number variation52estd199human GRCh37 chr7: 155,594,945-155,608,992 , GRCh38.p12 chr7: 155,802,251-155,816,298 SHH
    esv2675982copy number variation92estd199human GRCh37 chr8: 21,624,845-21,638,692 , GRCh38.p12 chr8: 21,767,333-21,781,180 GFRA2
    esv2665595copy number variation24estd199human GRCh37 chr18: 66,745,845-66,758,892 , GRCh38.p12 chr18: 69,078,608-69,091,655 CCDC102B
    esv2669985copy number variation97estd199human GRCh37 chr19: 1,852,045-1,864,992 , GRCh38.p12 chr19: 1,852,046-1,864,993 KLF16
    esv2659442copy number variation87estd199human GRCh37 chr7: 150,945-159,992 , GRCh38.p12 chr7: 150,945-159,992 , GRCh38.p12 chr7|NT_187558.1: 106,750-119,335 , GRCh38.p12 chr7|NT_187653.1: 143,266-152,313 LINC03014
    esv2675866copy number variation315estd199human GRCh37 chr9: 113,024,576-113,037,093 , GRCh38.p12 chr9: 110,262,296-110,274,813 LOC107987114
    esv2656873copy number variation10estd199human GRCh37 chr12: 6,813,695-6,825,392 , GRCh38.p12 chr12: 6,704,529-6,716,226 RNU6-781P
    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