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 154

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096696copy number variation1nstd102humanUncertain significance GRCh37 chr3: 14,180,660-14,180,817 , GRCh38.p12 chr3: 14,139,160-14,139,317 TMEM43
    nsv6714894copy number variation1nstd229human GRCh38 chr3: 14,064,301-14,499,300 , GRCh37.p13 chr3: 14,105,801-14,540,808 TMEM43, SLC6A6, 11 more genes
    nsv6710641copy number variation1nstd229human GRCh38 chr3: 14,136,686-14,137,363 , GRCh37.p13 chr3: 14,178,186-14,178,863 TMEM43
    nsv6701112copy number variation1nstd229human GRCh38 chr3: 12,689,301-14,136,700 , GRCh37.p13 chr3: 12,730,800-14,178,200 SNORA93, LOC105376957, 28 more genes
    nsv6700261copy number variation1nstd229human GRCh38 chr3: 14,133,713-14,141,666 , GRCh37.p13 chr3: 14,175,213-14,183,166 TMEM43
    nsv6634486copy number variation1nstd102humanLikely benign GRCh37 chr3: 14,178,181-14,178,856 , GRCh38 chr3: 14,136,681-14,137,356 TMEM43
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6368223copy number variation1nstd223human GRCh38 chr3: 14,138,735-14,140,255 , GRCh37.p13 chr3: 14,180,235-14,181,755 TMEM43
    nsv6355901copy number variation1nstd223human GRCh38 chr3: 14,136,686-14,137,356 , GRCh37.p13 chr3: 14,178,186-14,178,856 TMEM43
    nsv6315249copy number variation1nstd102humanPathogenic GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998 RNU6-905P, PRR3P1, 99 more genes
    nsv6311955copy number variation1nstd102humanUncertain significance GRCh37 chr3: 14,166,694-14,183,295 , GRCh38.p12 chr3: 14,125,194-14,141,795 CHCHD4, TMEM43
    nsv6299907copy number variation1nstd186human GRCh37 chr3: 14,181,973-14,182,064 , GRCh38.p12 chr3: 14,140,473-14,140,564 TMEM43
    nsv5991343copy number variation1nstd212human GRCh38 chr3: 14,136,680-14,137,356 , GRCh37.p13 chr3: 14,178,180-14,178,856 TMEM43
    nsv5893876copy number variation1nstd209human GRCh38 chr3: 14,136,680-14,137,355 , GRCh37.p13 chr3: 14,178,180-14,178,855 TMEM43
    nsv5673474copy number variation1nstd102humanPathogenic GRCh37 chr3: 14,166,684-14,220,439 , GRCh38.p12 chr3: 14,125,184-14,178,939 XPC, TMEM43, 3 more genes
    nsv5570342copy number variation1nstd207human GRCh38 chr3: 14,136,680-14,137,355 , GRCh37.p13 chr3: 14,178,180-14,178,855 TMEM43
    nsv5452866copy number variation1nstd206human GRCh38 chr3: 14,140,473-14,140,564 , GRCh37.p13 chr3: 14,181,973-14,182,064 TMEM43
    nsv5434375copy number variation1nstd206human GRCh38 chr3: 14,136,686-14,137,356 , GRCh37.p13 chr3: 14,178,186-14,178,856 TMEM43
    nsv5388407copy number variation2nstd186human GRCh37 chr3: 14,178,186-14,178,856 , GRCh38.p12 chr3: 14,136,686-14,137,356 TMEM43
    nsv5327466translocation1nstd204human GRCh38.p13 chr3: 14,136,686-14,136,686 , GRCh38.p13 chr3: 14,137,356-14,137,356 , GRCh37.p13 chr3: 14,178,186-14,178,186 , GRCh37.p13 chr3: 14,178,856-14,178,856 TMEM43
    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