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 142

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv6937226copy number variation1nstd229human GRCh38 chr12: 125,983,721-126,149,036 , GRCh37.p13 chr12: 126,468,267-126,633,582 LINC02826, LOC107984447, 4 more genes
    nsv6936540copy number variation1nstd229human GRCh38 chr12: 125,689,112-126,197,982 , GRCh37.p13 chr12: 126,173,658-126,682,528 LINC00939, LOC100420118, 7 more genes
    nsv6929652copy number variation1nstd229human GRCh38 chr12: 125,618,858-125,971,004 , GRCh37.p13 chr12: 126,103,404-126,455,550 TMEM132B, LINC00939, 2 more genes
    nsv6920779copy number variation1nstd229human GRCh38 chr12: 125,976,601-126,022,000 , GRCh37.p13 chr12: 126,461,147-126,506,546 LINC02826, LINC00939, 2 more genes
    nsv6919603copy number variation1nstd229human GRCh38 chr12: 125,966,701-126,005,941 , GRCh37.p13 chr12: 126,451,247-126,490,487 LINC00939, LOC105370058, 1 more genes
    nsv6491452copy number variation1nstd223human GRCh38 chr12: 125,983,721-126,149,033 , GRCh37.p13 chr12: 126,468,267-126,633,579 LINC00939, LINC02359, 4 more genes
    nsv6489865copy number variation1nstd223human GRCh38 chr12: 125,955,841-125,972,434 , GRCh37.p13 chr12: 126,440,387-126,456,980 LINC00939
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6132222copy number variation1nstd213human GRCh37 chr12: 126,430,000-126,670,001 , GRCh38.p12 chr12: 125,945,454-126,185,455 , LINC00939, 5 more genes
    nsv6132144copy number variation1nstd213human GRCh37 chr12: 126,350,000-126,480,001 , GRCh38.p12 chr12: 125,865,454-125,995,455 LINC00939, LOC100419701, 2 more genes
    nsv5381782copy number variation1nstd102humanPathogenic GRCh37 chr12: 123,878,845-126,829,341 , GRCh38.p12 chr12: 123,394,298-126,344,795 DDX55, ZNF664, 55 more genes
    nsv4529464copy number variation1nstd166human GRCh37.p13 chr12: 126,464,999-126,727,000 , GRCh38.p12 chr12: 125,980,453-126,242,454 , LINC00939, 6 more genes
    nsv4508775mobile element insertion1nstd166human GRCh37.p13 chr12: 126,452,250-126,452,250 , GRCh38.p12 chr12: 125,967,704-125,967,704 LINC00939
    nsv4455692copy number variation1nstd102humanPathogenic GRCh37 chr12: 122,169,403-129,084,163 , GRCh38.p12 chr12: 121,731,497-128,599,618 LOC107987176, LRRC43, 147 more genes
    nsv4385263copy number variation1nstd173human GRCh37 chr12: 126,463,562-126,727,689 , GRCh38.p12 chr12: 125,979,016-126,243,143 , LINC00939, 6 more genes
    nsv4384450copy number variation1nstd173human GRCh37 chr12: 126,463,562-126,720,475 , GRCh38.p12 chr12: 125,979,016-126,235,929 , LOC100420118, 6 more genes
    nsv4370349copy number variation1nstd173human GRCh37 chr12: 126,463,562-126,726,862 , GRCh38.p12 chr12: 125,979,016-126,242,316 , LINC02359, 6 more genes
    nsv4349911copy number variation1nstd102humanPathogenic GRCh37 chr12: 125,451,405-133,810,935 , GRCh38.p12 chr12: 124,966,859-133,234,349 LOC107987177, GOLGA3, 159 more genes
    nsv4230396copy number variation1nstd166human GRCh37.p13 chr12: 126,440,356-126,457,015 , GRCh38.p12 chr12: 125,955,810-125,972,469 LINC00939
    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