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 213

    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
    nsv7074465inversion1nstd229human GRCh38 chr19: 38,361,530-38,361,627 , GRCh37.p13 chr19: 38,852,170-38,852,267 CATSPERG
    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
    nsv7003208copy number variation1nstd229human GRCh38 chr19: 38,339,990-38,342,873 , GRCh37.p13 chr19: 38,830,630-38,833,513 CATSPERG
    nsv7001479copy number variation1nstd229human GRCh38 chr19: 38,337,758-38,341,895 , GRCh37.p13 chr19: 38,828,398-38,832,535 CATSPERG
    nsv7000667copy number variation1nstd229human GRCh38 chr19: 38,363,088-38,373,876 , GRCh37.p13 chr19: 38,853,728-38,864,516 PSMD8, CATSPERG
    nsv6528802copy number variation1nstd223human GRCh38 chr19: 37,602,649-38,484,499 , GRCh37.p13 chr19: 38,093,550-38,975,139 SPRED3, PSMD8, 30 more genes
    nsv6519847copy number variation1nstd223human GRCh38 chr19: 38,339,956-38,342,937 , GRCh37.p13 chr19: 38,830,596-38,833,577 CATSPERG
    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
    nsv6219869copy number variation1nstd214human GRCh38 chr19: 38,344,661-38,344,760 , GRCh37.p13 chr19: 38,835,301-38,835,400 CATSPERG
    nsv6208020copy number variation1nstd214human GRCh38 chr19: 38,344,661-38,344,735 , GRCh37.p13 chr19: 38,835,301-38,835,375 CATSPERG
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6101032insertion1nstd212human GRCh38 chr19: 38,355,342-38,355,342 , GRCh37.p13 chr19: 38,845,982-38,845,982 CATSPERG
    nsv6054681copy number variation1nstd212human GRCh38 chr19: 38,344,694-38,344,792 , GRCh37.p13 chr19: 38,835,334-38,835,432 CATSPERG
    nsv6051312copy number variation1nstd212human GRCh38 chr19: 38,347,886-38,351,541 , GRCh37.p13 chr19: 38,838,526-38,842,181 CATSPERG
    nsv5975329insertion1nstd209human GRCh38 chr19: 38,344,883-38,344,883 , GRCh37.p13 chr19: 38,835,523-38,835,523 CATSPERG
    nsv5940174copy number variation1nstd209human GRCh38 chr19: 38,353,420-38,353,733 , GRCh37.p13 chr19: 38,844,060-38,844,373 CATSPERG
    nsv5932595copy number variation1nstd209human GRCh38 chr19: 38,353,652-38,355,651 , GRCh37.p13 chr19: 38,844,292-38,846,291 CATSPERG
    nsv5876394copy number variation1nstd209human GRCh38 chr19: 38,353,960-38,355,561 , GRCh37.p13 chr19: 38,844,600-38,846,201 CATSPERG
    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