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 142

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147309insertion1nstd232human GRCh37.p13 chr19: 8,003,083-8,003,083 , GRCh38.p12 chr19: 7,938,198-7,938,198 TIMM44
    nsv7143914insertion1nstd232human GRCh37.p13 chr19: 7,999,126-7,999,126 , GRCh38.p12 chr19: 7,934,241-7,934,241 TIMM44
    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
    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
    nsv7000540copy number variation1nstd229human GRCh38 chr19: 7,936,903-7,936,960 , GRCh37.p13 chr19: 8,001,788-8,001,845 TIMM44
    nsv6998535copy number variation1nstd229human GRCh38 chr19: 7,936,906-7,936,960 , GRCh37.p13 chr19: 8,001,791-8,001,845 TIMM44
    nsv6205679copy number variation1nstd214human GRCh38 chr19: 7,936,903-7,936,959 , GRCh37.p13 chr19: 8,001,788-8,001,844 TIMM44
    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
    nsv5944872copy number variation1nstd209human GRCh38 chr19: 7,936,903-7,936,959 , GRCh37.p13 chr19: 8,001,788-8,001,844 TIMM44
    nsv5514946copy number variation1nstd206human GRCh38 chr19: 7,936,906-7,936,960 , GRCh37.p13 chr19: 8,001,791-8,001,845 TIMM44
    nsv5286741copy number variation1nstd204human GRCh38.p13 chr19: 7,941,246-7,943,545 , GRCh37.p13 chr19: 8,006,131-8,008,430 TIMM44
    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
    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