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 82

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3115219copy number variation3nstd145human GRCh37 chr5: 60,245,365-60,277,198 , GRCh38.p12 chr5: 60,949,538-60,981,371 NDUFAF2
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    nsv3112928copy number variation25nstd145human GRCh37 chr16: 60,082,253-60,098,427 , GRCh38.p12 chr16: 60,048,349-60,064,523 LINC02141
    nsv3117354copy number variation83nstd145human GRCh37 chr17: 15,043,995-15,058,468 , GRCh38.p12 chr17: 15,140,678-15,155,151 LOC107984976
    nsv3112217copy number variation43nstd145human GRCh37 chr4: 98,172,769-98,186,454 , GRCh38.p12 chr4: 97,251,618-97,265,303 STPG2
    nsv3118180copy number variation1nstd145human GRCh37 chr11: 125,797,556-125,811,120 , GRCh38.p12 chr11: 125,927,661-125,941,225 DDX25
    nsv3110986copy number variation37nstd145human GRCh37 chr5: 17,640,200-17,651,341 , GRCh38.p12 chr5: 17,640,091-17,651,232 LOC391768
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3111376copy number variation2nstd145human GRCh37 chr7: 91,033,585-91,040,956 , GRCh38.p12 chr7: 91,404,270-91,411,641 LINC02932
    nsv3114563copy number variation13nstd145human GRCh37 chr15: 32,509,181-32,514,993 , GRCh38.p12 chr15: 32,216,980-32,222,792 LOC102724078
    nsv3114628copy number variation1nstd145human GRCh37 chr10: 90,942,127-90,947,613 , GRCh38.p12 chr10: 89,182,370-89,187,856 LOC105378418
    nsv3110401copy number variation14nstd145human GRCh37 chr5: 11,129,609-11,134,869 , GRCh38.p12 chr5: 11,129,497-11,134,757 CTNND2
    nsv3114178copy number variation107nstd145human GRCh37 chr6: 53,928,991-53,933,879 , GRCh38.p12 chr6: 54,064,193-54,069,081 MLIP
    nsv3113139copy number variation39nstd145human GRCh37 chr13: 32,533,792-32,538,481 , GRCh38.p12 chr13: 31,959,655-31,964,344 EEF1DP3
    nsv3116148copy number variation97nstd145human GRCh37 chr8: 594,429-599,002 , GRCh38.p12 chr8: 644,429-649,002 ERICH1
    nsv3117725copy number variation19nstd145human GRCh37 chr6: 81,288,279-81,292,772 , GRCh38.p12 chr6: 80,578,562-80,583,055 LOC112267962
    nsv3114077copy number variation1nstd145human GRCh37 chr12: 82,140,186-82,144,203 , GRCh38.p12 chr12: 81,746,407-81,750,424 PPFIA2
    nsv3111942copy number variation2nstd145human GRCh37 chr19: 44,951,947-44,955,901 , GRCh38.p12 chr19: 44,447,759-44,451,715 ZNF229
    nsv3114844copy number variation1nstd145human GRCh37 chr5: 172,032,324-172,036,268 , GRCh38.p12 chr5: 172,605,321-172,609,265 LOC105377729
    nsv3110873copy number variation5nstd145human GRCh37 chr8: 127,984,394-127,988,082 , GRCh38.p12 chr8: 126,972,149-126,975,837 LOC105375751
    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