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 126

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6290212copy number variation1nstd102humanPathogenic GRCh37 chr12: 6,105,118-6,131,251 , GRCh38.p12 chr12: 5,995,952-6,022,085 VWF
    nsv6315268copy number variation1nstd102humanPathogenic GRCh37 chr12: 6,105,389-6,122,646 , GRCh38.p12 chr12: 5,996,223-6,013,480 VWF
    nsv5564375copy number variation1nstd102humanPathogenic GRCh37 chr12: 6,220,135-6,233,842 , GRCh38.p12 chr12: 6,110,969-6,124,676 VWF
    nsv5564130copy number variation1nstd102humanPathogenic GRCh37 chr12: 6,161,950-6,172,119 , GRCh38.p12 chr12: 6,052,784-6,062,953 VWF
    nsv5380731copy number variation3nstd102humanPathogenic, not provided GRCh38 chr12: 6,103,315-6,111,945 , GRCh37 chr12: 6,212,481-6,221,111 VWF
    nsv5564209copy number variation1nstd102humanPathogenic GRCh37 chr12: 6,153,618-6,161,708 , GRCh38.p12 chr12: 6,044,452-6,052,542 VWF
    nsv7097699copy number variation1nstd102humanPathogenic GRCh37 chr9: 136,287,564-136,291,485 , GRCh38.p12 chr9: 133,422,444-133,426,365 , GRCh38.p12 chr9|NW_009646201.1: 248,538-252,459 ADAMTS13
    nsv6290218copy number variation1nstd102humanPathogenic GRCh37 chr12: 6,120,733-6,121,346 , GRCh38 chr12: 6,011,567-6,012,180 VWF
    nsv6290011delins1nstd102humanPathogenic GRCh37 chr12: 6,128,479-6,128,749 , GRCh38.p12 chr12: 6,019,313-6,019,583 VWF
    nsv6290019delins1nstd102humanPathogenic GRCh37 chr12: 6,128,633-6,128,795 , GRCh38.p12 chr12: 6,019,467-6,019,629 VWF
    nsv5672788copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 6,212,062-6,221,814 , GRCh38 chr12: 6,102,896-6,112,648 VWF
    nsv5672642copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 6,212,480-6,221,111 , GRCh38 chr12: 6,103,314-6,111,945 VWF
    nsv3896892copy number variation1nstd102humanBenign GRCh37 chr9: 136,291,361-136,316,040 , GRCh38.p12 chr9: 133,426,241-133,450,919 , GRCh38.p12 chr9|NW_009646201.1: 252,335-277,013 ADAMTS13
    nsv3900631copy number variation1nstd102humanBenign GRCh37 chr12: 6,232,426-6,246,446 , GRCh38.p12 chr12: 6,123,260-6,137,280 VWF
    nsv4455343copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,120,583-6,136,914 , GRCh38.p12 chr12: 6,011,417-6,027,748 VWF
    nsv6314967delins1nstd102humanUncertain significance GRCh38 chr12: 6,019,583-6,019,732 , GRCh37.p13 chr12: 6,128,749-6,128,898 VWF
    nsv6314966delins1nstd102humanUncertain significance GRCh38 chr12: 6,019,621-6,019,732 , GRCh37.p13 chr12: 6,128,787-6,128,898 VWF
    nsv6314965delins1nstd102humanUncertain significance GRCh38 chr12: 6,019,283-6,019,391 , GRCh37.p13 chr12: 6,128,449-6,128,557 VWF
    nsv6314968delins1nstd102humanUncertain significance GRCh38 chr12: 6,019,621-6,019,683 , GRCh37.p13 chr12: 6,128,787-6,128,849 VWF
    nsv6314971delins1nstd102humanUncertain significance GRCh38 chr12: 6,019,283-6,019,339 , GRCh37.p13 chr12: 6,128,449-6,128,505 VWF
    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