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 23137

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5572397copy number variation1nstd207human GRCh38 chr4: 34,778,270-34,827,327 , GRCh37.p13 chr4: 34,779,892-34,828,949 LOC105378262
    nsv5594701copy number variation1nstd207human GRCh38 chr11: 3,290,735-3,336,551 , GRCh37.p13 chr11: 3,311,965-3,357,781 NDUFA5P1
    nsv5594292copy number variation1nstd207human GRCh38 chr20: 1,580,345-1,613,394 , GRCh37.p13 chr20: 1,560,991-1,594,040 SIRPB1
    nsv5604076copy number variation1nstd207human GRCh38 chr11: 1,894,042-1,915,724 , GRCh37.p13 chr11: 1,915,272-1,936,954 LINC01150
    nsv5581588copy number variation1nstd207human GRCh38 chr1: 207,545,410-207,563,965 , GRCh37.p13 chr1: 207,718,755-207,737,310 CR1
    nsv5568682copy number variation1nstd207human GRCh38 chr1: 207,526,605-207,545,159 , GRCh37.p13 chr1: 207,699,950-207,718,504 CR1
    nsv5572426copy number variation1nstd207human GRCh38 chr5: 156,048,921-156,063,029 , GRCh37.p13 chr5: 155,475,931-155,490,039 SGCD
    nsv5573610copy number variation1nstd207human GRCh38 chr7: 134,100,247-134,113,575 , GRCh37.p13 chr7: 133,785,000-133,798,328
    nsv5589051copy number variation1nstd207human GRCh38 chr16: 78,337,741-78,351,000 , GRCh37.p13 chr16: 78,371,638-78,384,897 WWOX
    nsv5567975copy number variation1nstd207human GRCh38 chr7: 100,729,949-100,743,092 , GRCh37.p13 chr7: 100,327,572-100,340,715 ZAN
    nsv5592689copy number variation1nstd207human GRCh38 chr13: 63,650,503-63,663,466 , GRCh37.p13 chr13: 64,224,636-64,237,599 LOC105370236
    nsv5588520copy number variation1nstd207human GRCh38 chr15: 76,592,255-76,604,596 , GRCh37.p13 chr15: 76,884,596-76,896,937 SCAPER
    nsv5566086copy number variation1nstd207human GRCh38 chr3: 52,993,164-53,004,881 , GRCh37.p13 chr3: 53,027,180-53,038,897 SFMBT1
    nsv5574543copy number variation1nstd207human GRCh38 chr8: 1,394,853-1,406,539 , GRCh37.p13 chr8: 1,343,019-1,354,705 DLGAP2
    nsv5599359copy number variation1nstd207human GRCh38 chr20: 54,030,525-54,041,462 , GRCh37.p13 chr20: 52,647,064-52,658,001 BCAS1
    nsv5573410copy number variation1nstd207human GRCh38 chr1: 34,635,820-34,646,374 , GRCh37.p13 chr1: 35,101,421-35,111,975 LOC105378641
    nsv5582351copy number variation1nstd207human GRCh38 chr3: 193,157,540-193,167,615 , GRCh37.p13 chr3: 192,875,329-192,885,404 VEZF1P1
    nsv5600622copy number variation1nstd207human GRCh38 chr9: 136,772,877-136,782,781 , GRCh37.p13 chr9: 139,667,329-139,677,233 ATP6V1G1P3
    nsv5575164copy number variation1nstd207human GRCh38 chr6: 80,574,001-80,583,859 , GRCh37.p13 chr6: 81,283,718-81,293,576 LOC112267962
    nsv5571414copy number variation1nstd207human GRCh38 chr6: 72,154,150-72,163,833 , GRCh37.p13 chr6: 72,863,853-72,873,536 RIMS1
    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