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 160

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098971copy number variation1nstd102humanUncertain significance GRCh37 chr8: 74,888,376-74,890,990 , GRCh38.p12 chr8: 73,976,141-73,978,755 TMEM70
    nsv7098183copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 74,890,971-74,891,116 , GRCh38.p12 chr8: 73,978,736-73,978,881 TMEM70
    nsv7077569inversion1nstd229human GRCh38 chr8: 72,847,163-78,693,142 , GRCh37.p13 chr8: 73,759,398-79,605,377 RDH10-AS1, PI15, 61 more genes
    nsv7072725inversion1nstd229human GRCh38 chr8: 73,250,658-74,373,186 , GRCh37.p13 chr8: 74,162,893-75,285,421 RPS20P21, C8orf89, 22 more genes
    nsv7064031inversion1nstd229human GRCh38 chr8: 72,138,738-75,988,244 , GRCh37.p13 chr8: 73,050,973-76,900,479 RNU6-1300P, RNU6-285P, 49 more genes
    nsv6858066copy number variation1nstd229human GRCh38 chr8: 73,912,974-74,271,181 , GRCh37.p13 chr8: 74,825,209-75,183,416 RPS3AP32, DSTNP3, 9 more genes
    nsv6851530copy number variation1nstd229human GRCh38 chr8: 73,978,587-73,978,620 , GRCh37.p13 chr8: 74,890,822-74,890,855 TMEM70
    nsv6850174copy number variation1nstd229human GRCh38 chr8: 73,867,372-74,551,526 , GRCh37.p13 chr8: 74,779,607-75,463,761 MIR5681A, JPH1, 14 more genes
    nsv6847327copy number variation1nstd229human GRCh38 chr8: 73,975,766-73,976,282 , GRCh37.p13 chr8: 74,888,001-74,888,517 TMEM70
    nsv6845648copy number variation1nstd229human GRCh38 chr8: 73,883,839-74,279,899 , GRCh37.p13 chr8: 74,796,074-75,192,134 LOC105375903, RNU6-1300P, 9 more genes
    nsv6843693copy number variation1nstd229human GRCh38 chr8: 73,976,049-73,976,104 , GRCh37.p13 chr8: 74,888,284-74,888,339 TMEM70
    nsv6637040copy number variation1nstd102humanUncertain significance GRCh37 chr8: 74,515,647-75,122,801 , GRCh38.p12 chr8: 73,603,412-74,210,566 STAU2, RN7SL760P, 13 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6575523inversion1nstd223human GRCh38 chr8: 72,881,788-80,095,071 , GRCh37.p13 chr8: 73,794,023-81,007,306 ZFHX4-AS1, LINC01111, 82 more genes
    nsv6558334inversion1nstd223human GRCh38 chr8: 73,974,185-73,974,902 , GRCh37.p13 chr8: 74,886,420-74,887,137 TMEM70
    nsv6422052copy number variation1nstd223human GRCh38 chr8: 73,973,637-73,975,404 , GRCh37.p13 chr8: 74,885,872-74,887,639 TMEM70
    nsv6420262copy number variation1nstd223human GRCh38 chr8: 73,867,372-74,551,522 , GRCh37.p13 chr8: 74,779,607-75,463,757 RNU6-1300P, LOC105375903, 14 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6312655copy number variation1nstd102humanPathogenic GRCh37 chr8: 74,890,971-74,903,809 , GRCh38.p12 chr8: 73,978,736-73,991,574 LY96, TMEM70, 2 more genes
    nsv6312654copy number variation2nstd102humanUncertain significance GRCh37 chr8: 74,888,517-75,276,602 , GRCh38.p12 chr8: 73,976,282-74,364,367 DSTNP3, JPH1, 8 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