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 226

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095479copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147 HNRNPL, RN7SL663P, 45 more genes
    nsv7095205copy number variation2nstd102humanUncertain significance GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932 CCNP, NFKBIB, 81 more genes
    nsv7077216inversion1nstd229human GRCh38 chr19: 39,031,980-39,032,141 , GRCh37.p13 chr19: 39,522,620-39,522,781 FBXO27
    nsv7075514inversion1nstd229human GRCh38 chr19: 38,994,526-39,502,034 , GRCh37.p13 chr19: 39,485,166-39,992,674 RPS16, PLEKHG2, 25 more genes
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7013705copy number variation1nstd229human GRCh38 chr19: 39,007,556-39,039,085 , GRCh37.p13 chr19: 39,498,196-39,529,725 FBXO27
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7002869copy number variation1nstd229human GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522 IFNL4P1, IFNL4, 19 more genes
    nsv6999803copy number variation1nstd229human GRCh38 chr19: 39,004,801-39,060,700 , GRCh37.p13 chr19: 39,495,441-39,551,340 FBXO27
    nsv6624468copy number variation1nstd224human GRCh37 chr19: 39,522,817-39,542,969 , GRCh38.p12 chr19: 39,032,177-39,052,329 FBXO27
    nsv6595968inversion1nstd223human GRCh38 chr19: 39,007,853-39,008,052 , GRCh37.p13 chr19: 39,498,493-39,498,692 FBXO27
    nsv6534149copy number variation1nstd223human GRCh38 chr19: 39,007,553-39,039,084 , GRCh37.p13 chr19: 39,498,193-39,529,724 FBXO27
    nsv6531882copy number variation1nstd223human GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522 NFKBIB, IFNL3, 19 more genes
    nsv6518593copy number variation1nstd223human GRCh38 chr19: 39,022,923-39,037,971 , GRCh37.p13 chr19: 39,513,563-39,528,611 FBXO27
    nsv6518047copy number variation1nstd223human GRCh38 chr19: 39,014,711-39,015,092 , GRCh37.p13 chr19: 39,505,351-39,505,732 FBXO27
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6285197insertion2nstd214human GRCh38 chr19: 39,031,690-39,031,690 , GRCh37.p13 chr19: 39,522,330-39,522,330 FBXO27
    nsv6251038mobile element insertion1nstd215human GRCh38 chr19: 39,020,772-39,020,772 , GRCh37.p13 chr19: 39,511,412-39,511,412 FBXO27
    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