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 128

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5485338copy number variation1nstd206human GRCh38 chr8: 66,427,917-66,428,620 , GRCh37.p13 chr8: 67,340,152-67,340,855 LOC102724687, RRS1-DT, 1 more genes
    nsv5317589copy number variation1nstd204human GRCh38.p13 chr8: 66,411,276-66,741,302 , GRCh37.p13 chr8: 67,323,511-67,653,537 C8orf44, RRS1-DT, 11 more genes
    nsv5258948copy number variation1nstd204human GRCh38.p13 chr8: 66,411,201-66,741,300 , GRCh37.p13 chr8: 67,323,436-67,653,535 MYBL1, SGK3, 11 more genes
    nsv5244624copy number variation1nstd204human GRCh38.p13 chr8: 66,411,289-66,448,607 , GRCh37.p13 chr8: 67,323,524-67,360,842 RRS1, RRS1-DT, 2 more genes
    nsv4965406copy number variation1nstd200human GRCh38 chr8: 66,411,286-66,741,296 , GRCh37.p13 chr8: 67,323,521-67,653,531 VCPIP1, RRS1-DT, 11 more genes
    nsv4960704copy number variation1nstd200human GRCh38 chr8: 66,427,917-66,428,620 , GRCh37.p13 chr8: 67,340,152-67,340,855 RRS1, LOC102724687, 1 more genes
    nsv4829064copy number variation1nstd200human GRCh37 chr8: 67,323,521-67,653,531 , GRCh38.p12 chr8: 66,411,286-66,741,296 VCPIP1, RRS1-DT, 11 more genes
    nsv4821782copy number variation1nstd200human GRCh37 chr8: 67,340,152-67,340,855 , GRCh38.p12 chr8: 66,427,917-66,428,620 RRS1-DT, RRS1, 1 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456190copy number variation1nstd102humanPathogenic GRCh37 chr8: 65,280,508-67,782,846 , GRCh38.p12 chr8: 64,367,951-66,870,611 BHLHE22-AS1, VCPIP1, 41 more genes
    nsv4387546copy number variation1nstd173human GRCh37 chr8: 65,023,339-68,301,135 , GRCh38.p12 chr8: 64,110,782-67,388,900 , LOC105375885, 56 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv3924415copy number variation1nstd102humanPathogenic GRCh37 chr8: 61,431,781-67,571,260 , GRCh38 chr8: 60,519,222-66,659,025 , NCBI36 chr8: 61,594,335-67,733,814 RN7SKP135, TRIM55, 77 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923011copy number variation1nstd102humanPathogenic GRCh38 chr8: 66,171,669-93,505,509 , GRCh37 chr8: 67,083,904-94,517,737 , NCBI36 chr8: 67,246,458-94,586,913 CA3, HAUS1P3, 353 more genes
    nsv3922631copy number variation1nstd102humanPathogenic GRCh38 chr8: 61,691,800-82,537,696 , NCBI36 chr8: 62,766,913-83,612,486 , GRCh37 chr8: 62,604,359-83,449,931 NCOA2, LOC107986893, 284 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 RPL5P22, ARHGEF10, 2105 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