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 366

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6890677copy number variation1nstd229human GRCh38 chr10: 11,895,082-11,901,819 , GRCh37.p13 chr10: 11,937,081-11,943,818 PROSER2-AS1
    nsv6884530copy number variation1nstd229human GRCh38 chr10: 11,831,553-11,836,260 , GRCh37.p13 chr10: 11,873,552-11,878,259 PROSER2
    nsv6890465copy number variation1nstd229human GRCh38 chr10: 11,834,308-11,838,216 , GRCh37.p13 chr10: 11,876,307-11,880,215 PROSER2
    nsv6891679copy number variation1nstd229human GRCh38 chr10: 11,818,268-11,821,706 , GRCh37.p13 chr10: 11,860,267-11,863,705 PROSER2
    nsv6890107copy number variation1nstd229human GRCh38 chr10: 11,841,988-11,843,454 , GRCh37.p13 chr10: 11,883,987-11,885,453 PROSER2
    nsv6894668copy number variation1nstd229human GRCh38 chr10: 11,893,209-11,893,253 , GRCh37.p13 chr10: 11,935,208-11,935,252 PROSER2-AS1
    nsv6441157copy number variation1nstd223human GRCh38 chr10: 11,895,082-11,901,817 , GRCh37.p13 chr10: 11,937,081-11,943,816 PROSER2-AS1
    nsv6447721copy number variation1nstd223human GRCh38 chr10: 11,820,295-11,826,785 , GRCh37.p13 chr10: 11,862,294-11,868,784 PROSER2
    nsv6439891copy number variation1nstd223human GRCh38 chr10: 11,831,553-11,836,258 , GRCh37.p13 chr10: 11,873,552-11,878,257 PROSER2
    nsv6453653copy number variation1nstd223human GRCh38 chr10: 11,837,708-11,840,343 , GRCh37.p13 chr10: 11,879,707-11,882,342 PROSER2
    nsv6449065copy number variation1nstd223human GRCh38 chr10: 11,888,399-11,889,594 , GRCh37.p13 chr10: 11,930,398-11,931,593 PROSER2-AS1
    nsv6443236copy number variation1nstd223human GRCh38 chr10: 11,833,606-11,834,650 , GRCh37.p13 chr10: 11,875,605-11,876,649 PROSER2
    nsv5491231copy number variation1nstd206human GRCh38 chr10: 11,832,797-11,833,142 , GRCh37.p13 chr10: 11,874,796-11,875,141 PROSER2
    nsv6266487copy number variation1nstd214human GRCh38 chr10: 11,885,317-11,885,511 , GRCh37.p13 chr10: 11,927,316-11,927,510 PROSER2-AS1
    nsv6172287copy number variation1nstd214human GRCh38 chr10: 11,885,373-11,885,528 , GRCh37.p13 chr10: 11,927,372-11,927,527 PROSER2-AS1
    nsv6269603copy number variation1nstd214human GRCh38 chr10: 11,885,296-11,885,412 , GRCh37.p13 chr10: 11,927,295-11,927,411 PROSER2-AS1
    nsv6267843copy number variation1nstd214human GRCh38 chr10: 11,885,356-11,885,472 , GRCh37.p13 chr10: 11,927,355-11,927,471 PROSER2-AS1
    nsv6178829copy number variation1nstd214human GRCh38 chr10: 11,885,361-11,885,477 , GRCh37.p13 chr10: 11,927,360-11,927,476 PROSER2-AS1
    nsv6170625copy number variation1nstd214human GRCh38 chr10: 11,885,374-11,885,489 , GRCh37.p13 chr10: 11,927,373-11,927,488 PROSER2-AS1
    nsv6011173copy number variation1nstd212human GRCh38 chr10: 11,888,000-11,889,430 , GRCh37.p13 chr10: 11,929,999-11,931,429 PROSER2-AS1
    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