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 640

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6795417copy number variation1nstd229human GRCh38 chr5: 180,511,382-180,520,548 , GRCh37.p13 chr5: 179,938,382-179,947,548 CNOT6
    nsv6778698copy number variation1nstd229human GRCh38 chr5: 180,522,262-180,527,912 , GRCh37.p13 chr5: 179,949,262-179,954,912 CNOT6
    nsv6785258copy number variation1nstd229human GRCh38 chr5: 180,494,641-180,498,765 , GRCh37.p13 chr5: 179,921,641-179,925,765 CNOT6
    nsv6788444copy number variation1nstd229human GRCh38 chr5: 180,513,467-180,516,282 , GRCh37.p13 chr5: 179,940,467-179,943,282 CNOT6
    nsv6795708copy number variation1nstd229human GRCh38 chr5: 180,550,364-180,552,496 , GRCh37.p13 chr5: 179,977,364-179,979,496 CNOT6
    nsv6783829copy number variation1nstd229human GRCh38 chr5: 180,531,107-180,531,201 , GRCh37.p13 chr5: 179,958,107-179,958,201 CNOT6
    nsv6788102copy number variation1nstd229human GRCh38 chr5: 180,520,479-180,520,540 , GRCh37.p13 chr5: 179,947,479-179,947,540 CNOT6
    nsv6790587copy number variation1nstd229human GRCh38 chr5: 180,549,039-180,549,068 , GRCh37.p13 chr5: 179,976,039-179,976,068 CNOT6
    nsv6399147copy number variation1nstd223human GRCh38 chr5: 180,539,879-180,544,006 , GRCh37.p13 chr5: 179,966,879-179,971,006 CNOT6
    nsv6401234copy number variation1nstd223human GRCh38 chr5: 180,536,206-180,539,796 , GRCh37.p13 chr5: 179,963,206-179,966,796 CNOT6
    nsv6412142copy number variation1nstd223human GRCh38 chr5: 180,513,486-180,516,259 , GRCh37.p13 chr5: 179,940,486-179,943,259 CNOT6
    nsv6411610copy number variation1nstd223human GRCh38 chr5: 180,550,354-180,552,506 , GRCh37.p13 chr5: 179,977,354-179,979,506 CNOT6
    nsv6403123copy number variation1nstd223human GRCh38 chr5: 180,556,892-180,558,561 , GRCh37.p13 chr5: 179,983,892-179,985,561 CNOT6
    nsv6407314copy number variation1nstd223human GRCh38 chr5: 180,540,638-180,541,735 , GRCh37.p13 chr5: 179,967,638-179,968,735 CNOT6
    nsv6370300copy number variation1nstd223human GRCh38 chr3: 32,955,856-32,956,690 , GRCh37.p13 chr3: 32,997,348-32,998,182 CCR4
    nsv5463011copy number variation1nstd206human GRCh38 chr5: 180,550,363-180,552,506 , GRCh37.p13 chr5: 179,977,363-179,979,506 CNOT6
    nsv5468705copy number variation1nstd206human GRCh38 chr5: 180,531,144-180,531,201 , GRCh37.p13 chr5: 179,958,144-179,958,201 CNOT6
    nsv4644896copy number variation1nstd186human GRCh37 chr5: 179,958,144-179,958,201 , GRCh38.p12 chr5: 180,531,144-180,531,201 CNOT6
    nsv6017681copy number variation1nstd212human GRCh38 chr5: 180,531,117-180,531,213 , GRCh37.p13 chr5: 179,958,117-179,958,213 CNOT6
    nsv6010916copy number variation1nstd212human GRCh38 chr5: 180,539,551-180,539,605 , GRCh37.p13 chr5: 179,966,551-179,966,605 CNOT6
    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