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 793

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4456003copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,773,268-17,861,398 , GRCh38.p12 chr8: 17,915,759-18,003,889 PCM1
    esv4004046copy number variation1estd231human GRCh37 chr8: 17,859,497-17,860,422 , GRCh38.p12 chr8: 18,001,988-18,002,913 PCM1
    nsv6856142copy number variation1nstd229human GRCh38 chr8: 17,927,701-18,032,400 , GRCh37.p13 chr8: 17,785,210-17,889,909 PCM1
    nsv6855991copy number variation1nstd229human GRCh38 chr8: 17,932,901-17,958,100 , GRCh37.p13 chr8: 17,790,410-17,815,609 PCM1
    nsv6842211copy number variation1nstd229human GRCh38 chr8: 17,956,444-17,967,279 , GRCh37.p13 chr8: 17,813,953-17,824,788 PCM1
    nsv6842245copy number variation1nstd229human GRCh38 chr8: 18,010,801-18,021,000 , GRCh37.p13 chr8: 17,868,310-17,878,509 PCM1
    nsv6845448copy number variation1nstd229human GRCh38 chr8: 17,965,543-17,972,781 , GRCh37.p13 chr8: 17,823,052-17,830,290 PCM1
    nsv6849952copy number variation1nstd229human GRCh38 chr8: 17,950,123-17,956,438 , GRCh37.p13 chr8: 17,807,632-17,813,947 PCM1
    nsv6857601copy number variation1nstd229human GRCh38 chr8: 17,923,977-17,928,702 , GRCh37.p13 chr8: 17,781,486-17,786,211 PCM1
    nsv6850761copy number variation1nstd229human GRCh38 chr8: 17,951,933-17,956,593 , GRCh37.p13 chr8: 17,809,442-17,814,102 PCM1
    nsv6838531copy number variation1nstd229human GRCh38 chr8: 17,980,482-17,982,421 , GRCh37.p13 chr8: 17,837,991-17,839,930 PCM1
    nsv6852976copy number variation1nstd229human GRCh38 chr8: 17,994,716-17,995,752 , GRCh37.p13 chr8: 17,852,225-17,853,261 PCM1
    nsv7147343copy number variation1nstd232human GRCh37.p13 chr8: 17,882,960-17,883,049 , GRCh38.p12 chr8: 18,025,451-18,025,540 PCM1
    nsv6428000copy number variation1nstd223human GRCh38 chr8: 17,930,384-17,934,439 , GRCh37.p13 chr8: 17,787,893-17,791,948 PCM1
    nsv6427174copy number variation1nstd223human GRCh38 chr8: 17,994,716-17,995,749 , GRCh37.p13 chr8: 17,852,225-17,853,258 PCM1
    nsv6417486copy number variation1nstd223human GRCh38 chr8: 17,979,201-17,980,200 , GRCh37.p13 chr8: 17,836,710-17,837,709 PCM1
    nsv6427387copy number variation1nstd223human GRCh38 chr8: 17,970,101-17,971,000 , GRCh37.p13 chr8: 17,827,610-17,828,509 PCM1
    nsv5487216copy number variation1nstd206human GRCh38 chr8: 17,994,716-17,995,749 , GRCh37.p13 chr8: 17,852,225-17,853,258 PCM1
    nsv5482804copy number variation1nstd206human GRCh38 chr8: 18,001,995-18,002,913 , GRCh37.p13 chr8: 17,859,504-17,860,422 PCM1
    nsv5493739copy number variation1nstd206human GRCh38 chr8: 18,026,403-18,026,503 , GRCh37.p13 chr8: 17,883,912-17,884,012 PCM1
    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