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 836

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    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
    esv2666779copy number variation14estd199human GRCh37 chr2: 203,295,245-203,314,492 , GRCh38.p12 chr2: 202,430,522-202,449,769 BMPR2
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2670051copy number variation18estd199human GRCh37 chr10: 96,867,145-96,876,592 , GRCh38.p12 chr10: 95,107,388-95,116,835
    esv2673706copy number variation19estd199human GRCh37 chr5: 19,223,060-19,232,165 , GRCh38.p12 chr5: 19,222,951-19,232,056 HSPD1P15
    esv2663931copy number variation243estd199human GRCh37 chr4: 138,092,000-138,100,631 , GRCh38.p12 chr4: 137,170,846-137,179,477 LINC02511
    esv2658946copy number variation162estd199human GRCh37 chr10: 96,867,192-96,874,942 , GRCh38.p12 chr10: 95,107,435-95,115,185
    esv2671335copy number variation339estd199human GRCh37 chr15: 91,981,577-91,989,265 , GRCh38.p12 chr15: 91,438,347-91,446,035 LOC107984778
    esv2673888copy number variation44estd199human GRCh37 chr7: 102,366,700-102,374,330 , GRCh38.p12 chr7: 102,726,253-102,733,883 RASA4DP
    esv2662988copy number variation516estd199human GRCh37 chr12: 45,903,153-45,909,939 , GRCh38.p12 chr12: 45,509,370-45,516,156 LOC105369743
    esv2673118copy number variation530estd199human GRCh37 chr6: 136,582,615-136,589,299 , GRCh38.p12 chr6: 136,261,477-136,268,161 BCLAF1
    esv2656489copy number variation507estd199human GRCh37 chr9: 15,815,306-15,821,940 , GRCh38.p12 chr9: 15,815,308-15,821,942 CCDC171
    esv2659943copy number variation369estd199human GRCh37 chr1: 222,374,165-222,380,539 , GRCh38.p12 chr1: 222,200,823-222,207,197 CFAP144P3
    esv2660784copy number variation254estd199human GRCh37 chr19: 36,840,751-36,847,072 , GRCh38.p12 chr19: 36,349,849-36,356,170 ZFP14
    esv2658674copy number variation196estd199human GRCh37 chr19: 36,840,751-36,847,072 , GRCh38.p12 chr19: 36,349,849-36,356,170 ZFP14
    esv2674135copy number variation25estd199human GRCh37 chr8: 114,040,465-114,046,767 , GRCh38.p12 chr8: 113,028,236-113,034,538 CSMD3
    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