U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 403

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097562copy number variation1nstd102humanPathogenic GRCh37 chr6: 10,813,857-10,813,976 , GRCh38.p12 chr6: 10,813,624-10,813,743 MAK
    nsv7097306copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,770,324-10,770,483 , GRCh38.p12 chr6: 10,770,091-10,770,250 MAK
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7042773inversion1nstd229human GRCh38 chr6: 8,542,608-11,835,677 , GRCh37.p13 chr6: 8,542,841-11,835,910 LOC112267952, RNU1-64P, 51 more genes
    nsv6797534copy number variation1nstd229human GRCh38 chr6: 10,799,107-10,810,622 , GRCh37.p13 chr6: 10,799,340-10,810,855 MAK
    nsv6797154copy number variation1nstd229human GRCh38 chr6: 10,814,909-10,856,384 , GRCh37.p13 chr6: 10,815,142-10,856,617 MAK
    nsv6791922copy number variation1nstd229human GRCh38 chr6: 10,692,401-10,762,600 , GRCh37.p13 chr6: 10,692,634-10,762,833 MAK, TMEM14C, 4 more genes
    nsv6791624copy number variation1nstd229human GRCh38 chr6: 10,760,843-10,761,112 , GRCh37.p13 chr6: 10,761,076-10,761,345 MAK
    nsv6790934copy number variation1nstd229human GRCh38 chr6: 10,766,931-10,767,013 , GRCh37.p13 chr6: 10,767,164-10,767,246 MAK
    nsv6790364copy number variation1nstd229human GRCh38 chr6: 10,795,137-10,800,253 , GRCh37.p13 chr6: 10,795,370-10,800,486 MAK
    nsv6789320copy number variation1nstd229human GRCh38 chr6: 10,766,988-10,773,047 , GRCh37.p13 chr6: 10,767,221-10,773,280 MAK
    nsv6788449copy number variation1nstd229human GRCh38 chr6: 10,822,326-10,824,516 , GRCh37.p13 chr6: 10,822,559-10,824,749 MAK
    nsv6787926copy number variation1nstd229human GRCh38 chr6: 10,806,612-10,807,595 , GRCh37.p13 chr6: 10,806,845-10,807,828 MAK
    nsv6786002copy number variation1nstd229human GRCh38 chr6: 10,822,968-10,835,094 , GRCh37.p13 chr6: 10,823,201-10,835,327 MAK
    nsv6785829copy number variation1nstd229human GRCh38 chr6: 10,804,608-10,811,688 , GRCh37.p13 chr6: 10,804,841-10,811,921 MAK
    nsv6779523copy number variation1nstd229human GRCh38 chr6: 10,802,244-10,829,552 , GRCh37.p13 chr6: 10,802,477-10,829,785 MAK
    nsv6779065copy number variation1nstd229human GRCh38 chr6: 10,787,801-10,829,100 , GRCh37.p13 chr6: 10,788,034-10,829,333 MAK
    nsv6778453copy number variation1nstd229human GRCh38 chr6: 10,536,801-11,071,500 , GRCh37.p13 chr6: 10,537,034-11,071,733 TMEM14B, GCNT2, 13 more genes
    nsv6636124copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 10,804,125-10,813,876 , GRCh38.p12 chr6: 10,803,892-10,813,643 MAK
    nsv6573993inversion1nstd223human GRCh38 chr6: 10,814,075-10,814,591 , GRCh37.p13 chr6: 10,814,308-10,814,824 MAK
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    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