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 86

    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
    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
    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
    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
    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
    nsv4682037copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,587,617-8,373,194 , GRCh38.p12 chr19: 7,522,731-8,308,310 XAB2, CLEC4G, 40 more genes
    nsv4676269copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,657,490-8,569,762 , GRCh38.p12 chr19: 7,592,604-8,504,878 LRRC8E, CLEC4GP1, 47 more genes
    nsv4629101copy number variation1nstd183human GRCh37 chr19: 7,397,015-7,925,985 , GRCh38.p12 chr19: 7,332,094-7,861,099 , PEX11G, 27 more genes
    nsv4257097copy number variation1nstd166human GRCh37.p13 chr19: 7,786,000-7,836,900 , GRCh38.p12 chr19: 7,721,114-7,772,014 CLEC4M, CD209, 4 more genes
    nsv3968684copy number variation1nstd168human GRCh38 chr19: 7,709,461-7,727,455 , GRCh37.p13 chr19: 7,774,347-7,792,341 CLEC4G
    nsv3917314copy number variation1nstd102humanUncertain significance NCBI36 chr19: 7,145,928-7,798,318 , GRCh38 chr19: 7,194,917-7,827,432 , GRCh37 chr19: 7,194,928-7,892,318 CLEC4G, STXBP2, 26 more genes
    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