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 178

    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
    nsv7062626inversion1nstd229human GRCh38 chr10: 67,894,040-67,894,124 , GRCh37.p13 chr10: 69,653,798-69,653,882 SIRT1
    nsv6882629copy number variation1nstd229human GRCh38 chr10: 67,812,601-67,893,800 , GRCh37.p13 chr10: 69,572,359-69,653,558 DNAJC12, SIRT1, 4 more genes
    nsv6882508copy number variation1nstd229human GRCh38 chr10: 67,889,601-67,905,100 , GRCh37.p13 chr10: 69,649,359-69,664,857 SIRT1
    nsv6879964copy number variation1nstd229human GRCh38 chr10: 67,751,501-67,942,800 , GRCh37.p13 chr10: 69,511,259-69,702,557 RN7SL394P, RNU6-1250P, 9 more genes
    nsv6637501copy number variation1nstd102humanUncertain significance GRCh37 chr10: 69,575,390-69,911,592 , GRCh38.p12 chr10: 67,815,632-68,151,835 RN7SL220P, HERC4, 10 more genes
    nsv6593756inversion1nstd223human GRCh38 chr10: 67,904,161-67,904,714 , GRCh37.p13 chr10: 69,663,919-69,664,471 SIRT1
    nsv6585303inversion1nstd223human GRCh38 chr10: 67,896,963-67,897,294 , GRCh37.p13 chr10: 69,656,721-69,657,052 SIRT1
    nsv6580810inversion1nstd223human GRCh38 chr10: 67,899,963-67,900,213 , GRCh37.p13 chr10: 69,659,721-69,659,971 SIRT1
    nsv6580242inversion1nstd223human GRCh38 chr10: 67,890,345-67,890,898 , GRCh37.p13 chr10: 69,650,103-69,650,656 SIRT1
    nsv6447741copy number variation1nstd223human GRCh38 chr10: 67,893,274-67,896,316 , GRCh37.p13 chr10: 69,653,032-69,656,074 SIRT1
    nsv6445488copy number variation1nstd223human GRCh38 chr10: 67,884,201-67,885,700 , GRCh37.p13 chr10: 69,643,959-69,645,458 SIRT1
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 SLC25A16, CTNNA3, 204 more genes
    nsv6309157copy number variation1nstd102humanUncertain significance GRCh37 chr10: 69,644,213-69,651,332 , GRCh38.p12 chr10: 67,884,455-67,891,574 SIRT1
    nsv6308916copy number variation1nstd102humanUncertain significance GRCh37 chr10: 67,680,088-71,332,799 , GRCh38.p12 chr10: 65,920,330-69,573,043 RPS3AP38, MIR7151, 62 more genes
    nsv6305206copy number variation1nstd186human GRCh37 chr10: 69,656,453-69,657,018 , GRCh38.p12 chr10: 67,896,695-67,897,260 SIRT1
    nsv6131802copy number variation1nstd213human GRCh37 chr10: 69,550,000-69,830,001 , GRCh38.p12 chr10: 67,790,242-68,070,244 RPL21P92, HERC4, 10 more genes
    nsv5703944mobile element insertion1nstd211human GRCh38 chr10: 67,897,970-67,897,970 , GRCh37.p13 chr10: 69,657,728-69,657,728 SIRT1
    nsv5701180mobile element insertion1nstd211human GRCh38 chr10: 67,897,971-67,897,971 , GRCh37.p13 chr10: 69,657,729-69,657,729 SIRT1
    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