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 219

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099255copy number variation1nstd231human GRCh38.p12 chr1: 192,358,641-201,911,882 , GRCh37 chr1: 192,327,771-201,881,010 CACNA1S, CSRP1, 120 more genes
    nsv7057871inversion1nstd229human GRCh38 chr1: 191,728,426-196,575,913 , GRCh37.p13 chr1: 191,697,556-196,545,043 GLRX2, LOC107985241, 37 more genes
    nsv7044147inversion1nstd229human GRCh38 chr1: 190,518,287-195,020,156 , GRCh37.p13 chr1: 190,487,417-194,989,286 LOC105371668, B3GALT2, 34 more genes
    nsv6674267copy number variation1nstd229human GRCh38 chr1: 192,325,037-192,394,082 , GRCh37.p13 chr1: 192,294,167-192,363,212 RGS21
    nsv6673673copy number variation1nstd229human GRCh38 chr1: 192,296,387-192,333,710 , GRCh37.p13 chr1: 192,265,517-192,302,840 RGS21
    nsv6673153copy number variation1nstd229human GRCh38 chr1: 192,359,375-192,363,857 , GRCh37.p13 chr1: 192,328,505-192,332,987 RGS21
    nsv6671622copy number variation1nstd229human GRCh38 chr1: 192,344,037-192,344,222 , GRCh37.p13 chr1: 192,313,167-192,313,352 RGS21
    nsv6669761copy number variation1nstd229human GRCh38 chr1: 192,270,591-192,375,202 , GRCh37.p13 chr1: 192,239,721-192,344,332 RGS21
    nsv6664767copy number variation1nstd229human GRCh38 chr1: 192,297,258-192,325,026 , GRCh37.p13 chr1: 192,266,388-192,294,156 RGS21
    nsv6664098copy number variation1nstd229human GRCh38 chr1: 189,813,413-194,218,341 , GRCh37.p13 chr1: 189,782,543-194,187,471 RO60, MIR4426, 38 more genes
    nsv6662155copy number variation1nstd229human GRCh38 chr1: 192,311,502-192,318,216 , GRCh37.p13 chr1: 192,280,632-192,287,346 RGS21
    nsv6658702copy number variation1nstd229human GRCh38 chr1: 192,321,143-192,325,978 , GRCh37.p13 chr1: 192,290,273-192,295,108 RGS21
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6636659copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 189,633,885-199,854,163 , GRCh38.p12 chr1: 189,664,755-199,885,035 F13B, CFH, 88 more genes
    nsv6333348copy number variation1nstd223human GRCh38 chr1: 192,334,001-192,335,600 , GRCh37.p13 chr1: 192,303,131-192,304,730 RGS21
    nsv6333300copy number variation1nstd223human GRCh38 chr1: 192,349,648-192,350,175 , GRCh37.p13 chr1: 192,318,778-192,319,305 RGS21
    nsv6332732copy number variation1nstd223human GRCh38 chr1: 192,342,201-192,342,900 , GRCh37.p13 chr1: 192,311,331-192,312,030 RGS21
    nsv6330333copy number variation1nstd223human GRCh38 chr1: 192,360,515-192,361,180 , GRCh37.p13 chr1: 192,329,645-192,330,310 RGS21
    nsv6329318copy number variation1nstd223human GRCh38 chr1: 192,325,174-192,325,929 , GRCh37.p13 chr1: 192,294,304-192,295,059 RGS21
    nsv6328816copy number variation1nstd223human GRCh38 chr1: 192,316,801-192,318,200 , GRCh37.p13 chr1: 192,285,931-192,287,330 RGS21
    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