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 118

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7016488copy number variation1nstd229human GRCh38 chr19: 7,903,221-7,906,626 , GRCh37.p13 chr19: 7,968,106-7,971,511 MAP2K7
    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
    nsv7012552copy number variation1nstd229human GRCh38 chr19: 7,910,782-7,910,872 , GRCh37.p13 chr19: 7,975,667-7,975,757 MAP2K7
    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
    nsv7003572copy number variation1nstd229human GRCh38 chr19: 7,898,682-7,903,654 , GRCh37.p13 chr19: 7,963,567-7,968,539 MAP2K7, LRRC8E
    nsv6192404copy number variation1nstd214human GRCh38 chr19: 7,910,782-7,910,871 , GRCh37.p13 chr19: 7,975,667-7,975,756 MAP2K7
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133528copy number variation1nstd213human GRCh37 chr19: 7,780,000-8,030,001 , GRCh38.p12 chr19: 7,715,114-7,965,117 TIMM44, PRR36, 17 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv6126513copy number variation1nstd186human GRCh37 chr19: 7,976,032-7,982,974 , GRCh38.p12 chr19: 7,911,147-7,918,089 MAP2K7, TGFBR3L
    nsv6051300copy number variation1nstd212human GRCh38 chr19: 7,911,148-7,918,087 , GRCh37.p13 chr19: 7,976,033-7,982,972 MAP2K7, TGFBR3L
    nsv5932038copy number variation1nstd209human GRCh38 chr19: 7,910,782-7,910,871 , GRCh37.p13 chr19: 7,975,667-7,975,756 MAP2K7
    nsv5588670copy number variation1nstd207human GRCh38 chr19: 7,910,782-7,910,871 , GRCh37.p13 chr19: 7,975,667-7,975,756 MAP2K7
    nsv5519749copy number variation1nstd206human GRCh38 chr19: 7,911,147-7,918,089 , GRCh37.p13 chr19: 7,976,032-7,982,974 TGFBR3L, MAP2K7
    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