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 204

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137073copy number variation1nstd102humanPathogenic GRCh37 chr6: 491,126-1,624,775 , GRCh38.p12 chr6: 491,126-1,624,540 RN7SL352P, LOC107986555, 18 more genes
    nsv7137049copy number variation1nstd102humanPathogenic GRCh37 chr6: 393,153-3,751,765 , GRCh38.p12 chr6: 393,153-3,751,531 LOC105374883, LINC02525, 57 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv6796861copy number variation1nstd229human GRCh38 chr6: 1,309,463-1,584,108 , GRCh37.p13 chr6: 1,309,698-1,584,343 RN7SL352P, FOXF2-DT, 8 more genes
    nsv6791546copy number variation1nstd229human GRCh38 chr6: 1,355,405-2,241,325 , GRCh37.p13 chr6: 1,355,640-2,241,559 FOXF2-DT, LOC105374883, 11 more genes
    nsv6788945copy number variation1nstd229human GRCh38 chr6: 1,248,225-1,424,460 , GRCh37.p13 chr6: 1,248,460-1,424,695 FOXQ1, FOXF2, 4 more genes
    nsv6781953copy number variation1nstd229human GRCh38 chr6: 1,230,370-1,734,614 , GRCh37.p13 chr6: 1,230,605-1,734,848 LINC01394, LOC102723944, 13 more genes
    nsv6778808copy number variation1nstd229human GRCh38 chr6: 1,169,448-1,493,138 , GRCh37.p13 chr6: 1,169,683-1,493,373 LOC105374879, FOXF2-DT, 6 more genes
    nsv6636564copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,975-3,718,881 , GRCh38.p12 chr6: 156,975-3,718,647 LOC101927691, LOC107986555, 60 more genes
    nsv6630921copy number variation1nstd224human GRCh37 chr6: 1,149,856-1,613,686 , GRCh38.p12 chr6: 1,149,621-1,613,451 FOXF2, FOXCUT, 11 more genes
    nsv6408963copy number variation1nstd223human GRCh38 chr6: 1,232,014-1,776,081 , GRCh37.p13 chr6: 1,232,249-1,776,315 FOXC1, LOC102723944, 13 more genes
    nsv6400271copy number variation1nstd223human GRCh38 chr6: 1,248,224-1,424,459 , GRCh37.p13 chr6: 1,248,459-1,424,694 FOXF2, FOXQ1, 4 more genes
    nsv6398696copy number variation1nstd223human GRCh38 chr6: 1,205,201-1,848,200 , GRCh37.p13 chr6: 1,205,436-1,848,434 LOC105374879, FOXC1, 13 more genes
    nsv6314746copy number variation1nstd102humanPathogenic GRCh37 chr6: 375,263-3,655,142 , GRCh38.p12 chr6: 375,263-3,654,908 RN7SL352P, SERPINB8P1, 55 more genes
    nsv6313795copy number variation1nstd102humanUncertain significance GRCh37 chr6: 1,174,490-1,545,474 , GRCh38.p12 chr6: 1,174,255-1,545,239 RN7SL352P, LOC102723944, 8 more genes
    nsv6313679copy number variation1nstd102humanPathogenic GRCh37 chr6: 383,951-3,898,619 , GRCh38.p12 chr6: 383,951-3,898,385 SERPINB9P1, LOC101927691, 59 more genes
    nsv6290783copy number variation1nstd102humanUncertain significance GRCh37 chr6: 1,316,161-1,560,121 , GRCh38.p12 chr6: 1,315,926-1,559,886 LOC107986555, FOXF2, 7 more genes
    nsv6136505copy number variation1nstd213human GRCh37 chr6: 380,000-11,010,001 , GRCh38.p12 chr6: 380,000-11,009,768 BMP6, BPHL, 178 more genes
    nsv6135513copy number variation1nstd213human GRCh37 chr6: 380,000-10,980,001 , GRCh38.p12 chr6: 380,000-10,979,768 BMP6, BPHL, 178 more genes
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    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