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 172

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7073282inversion1nstd229human GRCh38 chr10: 12,099,288-14,830,781 , GRCh37.p13 chr10: 12,141,287-14,872,780 MIR1265, RNA5SP301, 45 more genes
    nsv7061969inversion1nstd229human GRCh38 chr10: 11,128,019-14,526,691 , GRCh37.p13 chr10: 11,169,982-14,568,690 RPL5P25, LOC105376425, 58 more genes
    nsv7060184inversion1nstd229human GRCh38 chr10: 13,148,010-16,128,795 , GRCh37.p13 chr10: 13,190,010-16,170,794 LOC101928453, MCM10, 52 more genes
    nsv7058695inversion1nstd229human GRCh38 chr10: 11,787,108-13,297,144 , GRCh37.p13 chr10: 11,829,107-13,339,144 RNU6-6P, SEC61A2, 28 more genes
    nsv6898000copy number variation1nstd229human GRCh38 chr10: 13,219,877-13,234,485 , GRCh37.p13 chr10: 13,261,877-13,276,485 UCMA
    nsv6896541copy number variation1nstd229human GRCh38 chr10: 13,210,947-13,223,143 , GRCh37.p13 chr10: 13,252,947-13,265,143 UCMA, RNU6-6P, 1 more genes
    nsv6891548copy number variation1nstd229human GRCh38 chr10: 13,208,500-13,222,996 , GRCh37.p13 chr10: 13,250,500-13,264,996 RNU6-6P, MCM10, 1 more genes
    nsv6882826copy number variation1nstd229human GRCh38 chr10: 13,222,751-13,226,257 , GRCh37.p13 chr10: 13,264,751-13,268,257 UCMA
    nsv6879878copy number variation1nstd229human GRCh38 chr10: 13,233,314-13,234,271 , GRCh37.p13 chr10: 13,275,314-13,276,271 UCMA
    nsv6879167copy number variation1nstd229human GRCh38 chr10: 13,231,928-13,234,256 , GRCh37.p13 chr10: 13,273,928-13,276,256 UCMA
    nsv6592458inversion1nstd223human GRCh38 chr10: 11,934,638-13,951,892 , GRCh37.p13 chr10: 11,976,637-13,993,892 RNU6-6P, MIR548Q, 38 more genes
    nsv6588427inversion1nstd223human GRCh38 chr10: 13,222,676-13,223,179 , GRCh37.p13 chr10: 13,264,676-13,265,179 UCMA
    nsv6452681copy number variation1nstd223human GRCh38 chr10: 13,210,947-13,223,140 , GRCh37.p13 chr10: 13,252,947-13,265,140 RNU6-6P, UCMA, 1 more genes
    nsv6445558copy number variation1nstd223human GRCh38 chr10: 13,229,497-13,230,996 , GRCh37.p13 chr10: 13,271,497-13,272,996 UCMA
    nsv6438579copy number variation1nstd223human GRCh38 chr10: 13,233,286-13,234,242 , GRCh37.p13 chr10: 13,275,286-13,276,242 UCMA
    nsv6438517copy number variation1nstd223human GRCh38 chr10: 13,232,369-13,235,558 , GRCh37.p13 chr10: 13,274,369-13,277,558 UCMA
    nsv6314829copy number variation1nstd102humanUncertain significance GRCh38 chr10: 13,233,315-13,234,242 , GRCh37 chr10: 13,275,315-13,276,242 UCMA
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 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