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 133

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142993copy number variation1nstd232human GRCh37.p13 chr11: 67,166,323-67,166,405 , GRCh38.p12 chr11: 67,398,852-67,398,934 PPP1CA, RAD9A
    nsv7139690copy number variation1nstd232human GRCh37.p13 chr11: 67,166,116-67,166,191 , GRCh38.p12 chr11: 67,398,645-67,398,720 PPP1CA, RAD9A
    nsv5503861copy number variation1nstd206human GRCh38 chr11: 67,401,916-67,401,990 , GRCh37.p13 chr11: 67,169,387-67,169,461 PPP1CA, TBC1D10C
    nsv6037184copy number variation1nstd212human GRCh38 chr11: 67,401,910-67,401,990 , GRCh37.p13 chr11: 67,169,381-67,169,461 TBC1D10C, PPP1CA
    nsv4208005copy number variation1nstd166human GRCh37.p13 chr11: 67,169,387-67,169,461 , GRCh38.p12 chr11: 67,401,916-67,401,990 PPP1CA, TBC1D10C
    esv3335687copy number variation1estd59human NCBI36 chr11: 66,924,652-66,927,100 , GRCh37.p13 chr11: 67,168,076-67,170,524 , GRCh38.p12 chr11: 67,400,605-67,403,053 PPP1CA, TBC1D10C
    esv3439784copy number variation8estd59human NCBI36 chr11: 66,924,777-66,927,325 , GRCh37.p13 chr11: 67,168,201-67,170,749 , GRCh38.p12 chr11: 67,400,730-67,403,278 PPP1CA, TBC1D10C
    esv1010387copy number variation1estd180human NCBI36 chr11: 66,920,403-66,921,230 , GRCh37.p13 chr11: 67,163,827-67,164,654 , GRCh38.p12 chr11: 67,396,356-67,397,183 RAD9A, PPP1CA
    esv2891624insertion1estd209human GRCh37 chr11: 67,165,217-67,165,217 , GRCh38.p12 chr11: 67,397,746-67,397,746 PPP1CA, RAD9A
    esv1456868insertion1estd22human NCBI36 chr11: 66,921,793-66,921,793 , GRCh37.p13 chr11: 67,165,217-67,165,217 , GRCh38.p12 chr11: 67,397,746-67,397,746 PPP1CA, RAD9A
    nsv5355313translocation1nstd200human GRCh38 chr11: 67,401,916-67,401,916 , GRCh38 chr11: 67,401,990-67,401,990 , GRCh37.p13 chr11: 67,169,461-67,169,461 , GRCh37.p13 chr11: 67,169,387-67,169,387 TBC1D10C, PPP1CA
    nsv5345380translocation1nstd200human GRCh37 chr11: 67,169,461-67,169,461 , GRCh37 chr11: 67,169,387-67,169,387 , GRCh38.p12 chr11: 67,401,990-67,401,990 , GRCh38.p12 chr11: 67,401,916-67,401,916 TBC1D10C, PPP1CA
    nsv3896716copy number variation1nstd102humanLikely benign GRCh37 chr11: 67,160,949-67,192,950 , GRCh38.p12 chr11: 67,393,478-67,425,479 RNU6-1238P, RAD9A, 3 more genes
    nsv3892870copy number variation1nstd102humanBenign GRCh37 chr11: 67,153,724-67,164,697 , GRCh38.p12 chr11: 67,386,253-67,397,226 RAD9A, LOC100130987, 2 more genes
    nsv3969325copy number variation1nstd168human GRCh38 chr11: 67,381,176-67,408,183 , GRCh37.p13 chr11: 67,148,647-67,175,654 RAD9A, TBC1D10C, 3 more genes
    nsv897810copy number variation1nstd71human NCBI36 chr11: 66,922,886-66,952,813 , GRCh37.p13 chr11: 67,166,310-67,196,237 , GRCh38.p12 chr11: 67,398,839-67,428,766 PPP1CA, TBC1D10C, 3 more genes
    nsv516453copy number variation4nstd21human NCBI35 chr11: 66,921,071-66,942,576 , GRCh37.p13 chr11: 67,164,495-67,186,000 , GRCh38.p12 chr11: 67,397,024-67,418,529 PPP1CA, RAD9A, 2 more genes
    nsv4203494copy number variation1nstd166human GRCh37.p13 chr11: 67,158,000-67,171,500 , GRCh38.p12 chr11: 67,390,529-67,404,029 LOC100130987, RAD9A, 3 more genes
    esv3977019copy number variation10estd229human GRCh37 chr11: 67,158,848-67,177,490 , GRCh38.p12 chr11: 67,391,377-67,410,019 PPP1CA, RAD9A, 3 more genes
    esv3977018copy number variation7estd229human GRCh37 chr11: 67,158,848-67,177,490 , GRCh38.p12 chr11: 67,391,377-67,410,019 PPP1CA, RAD9A, 3 more genes
    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