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 80

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3117131copy number variation1nstd145human GRCh37 chr9: 125,055,504-125,067,044 , GRCh38.p12 chr9: 122,293,225-122,304,765 MRRF
    nsv3111509copy number variation29nstd145human GRCh37 chr8: 2,150,517-2,161,441 , GRCh38.p12 chr8|NT_187576.1: 385,727-396,651 , GRCh38.p12 chr8: 2,202,878-2,213,774 LOC105377782
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3117920copy number variation33nstd145human GRCh37 chr17: 50,117,130-50,126,228 , GRCh38.p12 chr17: 52,039,770-52,048,868 CA10
    nsv3112428copy number variation41nstd145human GRCh37 chr1: 35,104,240-35,111,613 , GRCh38.p12 chr1: 34,638,639-34,646,012 LOC105378641
    nsv3112700copy number variation32nstd145human GRCh37 chr12: 86,695,674-86,703,013 , GRCh38.p12 chr12: 86,301,896-86,309,235 MGAT4C
    nsv3117823copy number variation1nstd145human GRCh37 chr17: 77,992,740-77,999,771 , GRCh38.p12 chr17: 80,018,941-80,025,972 TBC1D16
    nsv3115066copy number variation81nstd145human GRCh37 chr6: 19,042,250-19,049,222 , GRCh38.p12 chr6: 19,042,019-19,048,991 LOC105374958
    nsv3114114copy number variation1nstd145human GRCh37 chr20: 43,360,978-43,367,369 , GRCh38.p12 chr20: 44,732,337-44,738,728 KCNK15-AS1
    nsv3110559copy number variation79nstd145human GRCh37 chr2: 49,534,030-49,539,079 , GRCh38.p12 chr2: 49,306,891-49,311,940 LOC105374595
    nsv3114178copy number variation107nstd145human GRCh37 chr6: 53,928,991-53,933,879 , GRCh38.p12 chr6: 54,064,193-54,069,081 MLIP
    nsv3115871copy number variation21nstd145human GRCh37 chr11: 99,647,381-99,652,155 , GRCh38.p12 chr11: 99,776,650-99,781,424 CNTN5
    nsv3112371copy number variation15nstd145human GRCh37 chr6: 81,287,765-81,292,398 , GRCh38.p12 chr6: 80,578,048-80,582,681 LOC112267962
    nsv3114222copy number variation54nstd145human GRCh37 chr12: 82,139,806-82,144,215 , GRCh38.p12 chr12: 81,746,027-81,750,436 PPFIA2
    nsv3114430copy number variation5nstd145human GRCh37 chr11: 92,968,157-92,972,554 , GRCh38.p12 chr11: 93,234,991-93,239,388 SLC36A4
    nsv3116345copy number variation23nstd145human GRCh37 chr11: 58,632,160-58,635,965 , GRCh38.p12 chr11: 58,864,687-58,868,492 GLYATL2
    nsv3115376copy number variation4nstd145human GRCh37 chr4: 97,623,228-97,626,646 , GRCh38.p12 chr4: 96,702,077-96,705,495 LINC02267
    nsv3115553copy number variation167nstd145human GRCh37 chr22: 37,143,594-37,146,950 , GRCh38.p12 chr22: 36,747,550-36,750,906 CACNG2-DT
    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