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 60

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3118313copy number variation5nstd145human GRCh37 chr2: 15,159,289-15,195,216 , GRCh38.p12 chr2: 15,019,165-15,055,092 NBAS
    nsv3110960copy number variation10nstd145human GRCh37 chr4: 69,435,444-69,456,801 , GRCh38.p12 chr4: 68,569,726-68,591,083 UGT2B17
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3118025copy number variation35nstd145human GRCh37 chr8: 15,402,271-15,412,465 , GRCh38.p12 chr8: 15,544,762-15,554,956 TUSC3
    nsv3117920copy number variation33nstd145human GRCh37 chr17: 50,117,130-50,126,228 , GRCh38.p12 chr17: 52,039,770-52,048,868 CA10
    nsv3110176copy number variation2nstd145human GRCh37 chr12: 43,019,583-43,027,293 , GRCh38.p12 chr12: 42,625,781-42,633,491 LINC02402
    nsv3112700copy number variation32nstd145human GRCh37 chr12: 86,695,674-86,703,013 , GRCh38.p12 chr12: 86,301,896-86,309,235 MGAT4C
    nsv3112270copy number variation2nstd145human GRCh37 chr10: 127,950,094-127,957,268 , GRCh38.p12 chr10: 126,261,525-126,268,699 ADAM12
    nsv3115066copy number variation81nstd145human GRCh37 chr6: 19,042,250-19,049,222 , GRCh38.p12 chr6: 19,042,019-19,048,991 LOC105374958
    nsv3110881copy number variation1nstd145human GRCh37 chr5: 12,810,868-12,817,131 , GRCh38.p12 chr5: 12,810,756-12,817,019 LOC105374657
    nsv3118135copy number variation1nstd145human GRCh37 chr12: 90,150,991-90,157,221 , GRCh38.p12 chr12: 89,757,214-89,763,444 LOC107984543
    nsv3116197copy number variation63nstd145human GRCh37 chr7: 151,606-157,474 , GRCh38.p12 chr7: 151,606-157,474 , GRCh38.p12 chr7|NT_187558.1: 107,411-113,280 , GRCh38.p12 chr7|NT_187653.1: 143,927-149,795 LINC03014
    nsv3118173copy number variation16nstd145human GRCh37 chr3: 192,875,554-192,881,128 , GRCh38.p12 chr3: 193,157,765-193,163,339 VEZF1P1
    nsv3112062copy number variation15nstd145human GRCh37 chr8: 594,429-598,996 , GRCh38.p12 chr8: 644,429-648,996 ERICH1
    nsv3115260copy number variation3nstd145human GRCh37 chr10: 19,032,759-19,036,680 , GRCh38.p12 chr10: 18,743,830-18,747,751 LOC105376440
    nsv3112242copy number variation1nstd145human GRCh37 chr21: 32,110,760-32,113,942 , GRCh38.p12 chr21: 30,738,442-30,741,624 KRTAP21-4P
    nsv3116703copy number variation6nstd145human GRCh37 chr1: 86,401,559-86,404,507 , GRCh38.p12 chr1: 85,935,876-85,938,824 COL24A1
    nsv3117902copy number variation1nstd145human GRCh37 chr1: 42,685,879-42,688,717 , GRCh38.p12 chr1: 42,220,208-42,223,046 FOXJ3
    nsv3113637copy number variation9nstd145human GRCh37 chr22: 22,486,370-22,489,147 , GRCh38.p12 chr22: 22,131,977-22,134,754 IGL
    nsv3112729copy number variation26nstd145human GRCh37 chr22: 37,144,518-37,146,950 , GRCh38.p12 chr22: 36,748,474-36,750,906 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