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 283

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146585insertion1nstd232human GRCh37.p13 chr19: 7,756,010-7,756,010 , GRCh38.p12 chr19: 7,691,124-7,691,124 FCER2
    nsv7095726copy number variation1nstd102humanPathogenic GRCh37 chr19: 6,361,586-8,212,364 , GRCh38.p12 chr19: 6,361,575-8,147,480 SLC25A23, LYPLA2P2, 77 more genes
    nsv7095676copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,586,521-8,670,595 , GRCh38.p12 chr19: 7,521,635-8,605,710 LRRC8E, ZNF414, 53 more genes
    nsv7070187inversion1nstd229human GRCh38 chr19: 6,518,823-8,315,881 , GRCh37.p13 chr19: 6,518,834-8,380,765 , ZNF557, 69 more genes
    nsv7066716inversion1nstd229human GRCh38 chr19: 6,518,017-8,344,162 , GRCh37.p13 chr19: 6,518,028-8,409,046 , STXBP2, 71 more genes
    nsv7062847inversion1nstd229human GRCh38 chr19: 7,473,530-8,349,302 , GRCh37.p13 chr19: 7,538,416-8,414,186 CERS4, LYPLA2P2, 47 more genes
    nsv7013524copy number variation1nstd229human GRCh38 chr19: 7,623,595-7,921,993 , GRCh37.p13 chr19: 7,688,481-7,986,878 STXBP2, LOC100129391, 24 more genes
    nsv7012889copy number variation1nstd229human GRCh38 chr19: 7,616,098-7,695,916 , GRCh37.p13 chr19: 7,680,984-7,760,802 MCEMP1, RETN, 9 more genes
    nsv7011964copy number variation1nstd229human GRCh38 chr19: 7,354,369-9,019,195 , GRCh37.p13 chr19: 7,419,271-9,129,871 , MCOLN1, 66 more genes
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv7008722copy number variation1nstd229human GRCh38 chr19: 7,653,504-7,737,408 , GRCh37.p13 chr19: 7,718,390-7,802,294 TRAPPC5, FCER2, 5 more genes
    nsv7007292copy number variation1nstd229human GRCh38 chr19: 7,692,602-7,692,743 , GRCh37.p13 chr19: 7,757,488-7,757,629 FCER2
    nsv7002791copy number variation1nstd229human GRCh38 chr19: 7,688,597-7,693,019 , GRCh37.p13 chr19: 7,753,483-7,757,905 FCER2
    nsv6625513copy number variation1nstd224human GRCh37 chr19: 7,761,802-7,872,768 , GRCh38.p12 chr19: 7,696,916-7,807,882 FCER2, CLEC4M, 7 more genes
    nsv6625331copy number variation1nstd224human GRCh37 chr19: 7,663,768-7,881,030 , GRCh38.p12 chr19: 7,598,882-7,816,144 FCER2, STXBP2, 18 more genes
    nsv6597659inversion1nstd223human GRCh38 chr19: 7,700,948-7,702,839 , GRCh37.p13 chr19: 7,765,834-7,767,725 LOC105372262, FCER2
    nsv6526921copy number variation1nstd223human GRCh38 chr19: 7,686,515-7,687,897 , GRCh37.p13 chr19: 7,751,401-7,752,783 FCER2, TRAPPC5
    nsv6281568copy number variation1nstd214human GRCh38 chr19: 7,688,879-7,688,942 , GRCh37.p13 chr19: 7,753,765-7,753,828 FCER2
    nsv6238417insertion1nstd214human GRCh38 chr19: 7,691,078-7,691,078 , GRCh37.p13 chr19: 7,755,964-7,755,964 FCER2
    nsv6231511insertion2nstd214human GRCh38 chr19: 7,691,124-7,691,124 , GRCh37.p13 chr19: 7,756,010-7,756,010 FCER2
    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