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 1553

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2668450copy number variation3estd199human GRCh37 chr9: 26,707,652-26,788,038 , GRCh38.p12 chr9: 26,707,654-26,788,040 LOC105376000
    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
    esv2661219copy number variation458estd199human GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103 SPIDR
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    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
    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
    esv2661760copy number variation42estd199human GRCh37 chr7: 62,965,045-62,979,392 , GRCh38.p12 chr7: 63,504,667-63,519,014 PHKG1P2
    esv2668407copy number variation98estd199human GRCh37 chr11: 55,445,645-55,459,892 , GRCh38.p12 chr11: 55,678,169-55,692,416 OR4P1P
    esv2675982copy number variation92estd199human GRCh37 chr8: 21,624,845-21,638,692 , GRCh38.p12 chr8: 21,767,333-21,781,180 GFRA2
    esv2657895copy number variation46estd199human GRCh37 chr15: 76,883,645-76,897,492 , GRCh38.p12 chr15: 76,591,304-76,605,151 SCAPER
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2664165copy number variation220estd199human GRCh37 chr7: 100,327,572-100,340,716 , GRCh38.p12 chr7: 100,729,949-100,743,093 ZAN
    esv2659146copy number variation109estd199human GRCh37 chrX: 154,790,189-154,803,312 , GRCh38.p12 chrX: 155,560,528-155,573,651 TMLHE
    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