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 201

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7040565inversion1nstd229human GRCh38 chr5: 65,352,482-65,851,740 , GRCh37.p13 chr5: 64,648,309-65,147,568 LOC100419549, RPS2P23, 9 more genes
    nsv6777129copy number variation1nstd229human GRCh38 chr5: 65,517,434-66,063,747 , GRCh37.p13 chr5: 64,813,261-65,359,575 TRIM23, RNU6-540P, 9 more genes
    nsv6773652copy number variation1nstd229human GRCh38 chr5: 65,589,243-65,601,299 , GRCh37.p13 chr5: 64,885,070-64,897,126 TRIM23
    nsv6771381copy number variation1nstd229human GRCh38 chr5: 65,592,049-65,593,583 , GRCh37.p13 chr5: 64,887,876-64,889,410 TRIM23
    nsv6766966copy number variation1nstd229human GRCh38 chr5: 65,605,959-65,608,887 , GRCh37.p13 chr5: 64,901,786-64,904,714 TRIM23
    nsv6765694copy number variation1nstd229human GRCh38 chr5: 65,469,125-65,655,579 , GRCh37.p13 chr5: 64,764,952-64,951,406 PPWD1, SHLD3, 5 more genes
    nsv6765339copy number variation1nstd229human GRCh38 chr5: 65,595,125-65,604,197 , GRCh37.p13 chr5: 64,890,952-64,900,024 RNU6-540P, TRIM23
    nsv6765273copy number variation1nstd229human GRCh38 chr5: 65,460,432-65,973,179 , GRCh37.p13 chr5: 64,756,259-65,269,007 NLN, RNU6-540P, 10 more genes
    nsv6763313copy number variation1nstd229human GRCh38 chr5: 65,613,124-65,679,218 , GRCh37.p13 chr5: 64,908,951-64,975,045 TRAPPC13, SHLD3, 2 more genes
    nsv6569640inversion1nstd223human GRCh38 chr5: 65,616,640-65,616,818 , GRCh37.p13 chr5: 64,912,467-64,912,645 TRIM23
    nsv6566584inversion1nstd223human GRCh38 chr5: 65,592,366-65,593,304 , GRCh37.p13 chr5: 64,888,193-64,889,131 TRIM23
    nsv6557423inversion1nstd223human GRCh38 chr5: 65,616,562-65,616,903 , GRCh37.p13 chr5: 64,912,389-64,912,730 TRIM23
    nsv6555862inversion1nstd223human GRCh38 chr5: 65,621,356-65,621,849 , GRCh37.p13 chr5: 64,917,183-64,917,676 TRIM23
    nsv6395942copy number variation1nstd223human GRCh38 chr5: 65,589,243-65,601,296 , GRCh37.p13 chr5: 64,885,070-64,897,123 TRIM23
    nsv6313676copy number variation1nstd102humanPathogenic GRCh37 chr5: 64,049,692-70,306,646 , GRCh38.p12 chr5: 64,753,865-71,010,819 BCL9P1, CWC27, 105 more genes
    nsv6312114copy number variation1nstd102humanPathogenic GRCh37 chr5: 63,256,278-65,374,358 , GRCh38.p12 chr5: 63,960,451-66,078,530 RNF180, RPEP1, 23 more genes
    nsv6136128copy number variation1nstd213human GRCh37 chr5: 62,820,000-66,080,001 , GRCh38.p12 chr5: 63,524,173-66,784,173 TRIM23, HTR1A, 33 more genes
    nsv6135416copy number variation1nstd213human GRCh37 chr5: 50,510,000-68,870,001 , GRCh38.p12 chr5: 51,214,166-69,574,174 , TRIM23, 243 more genes
    nsv6135192copy number variation1nstd213human GRCh37 chr5: 63,780,000-66,290,001 , GRCh38.p12 chr5: 64,484,173-66,994,173 TRIM23, CWC27, 29 more genes
    nsv6065289insertion1nstd212human GRCh38 chr5: 65,590,694-65,590,694 , GRCh37.p13 chr5: 64,886,521-64,886,521 TRIM23
    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