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 145

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906739copy number variation1nstd209human GRCh38 chr6: 33,161,196-33,161,253 , GRCh37.p13 chr6: 33,128,973-33,129,030 COL11A2
    nsv5625003insertion1nstd207human GRCh38 chr6: 33,168,257-33,168,257 , GRCh37.p13 chr6: 33,136,034-33,136,034 COL11A2
    nsv5581824copy number variation1nstd207human GRCh38 chr6: 33,161,196-33,161,253 , GRCh37.p13 chr6: 33,128,973-33,129,030 COL11A2
    nsv5462197copy number variation1nstd206human GRCh38 chr6: 33,161,198-33,161,254 , GRCh37.p13 chr6: 33,128,975-33,129,031 COL11A2
    nsv5317483copy number variation1nstd204human GRCh38.p13 chr6: 33,146,352-33,172,284 , GRCh37.p13 chr6: 33,114,129-33,140,061 COL11A2, HCG24
    nsv5231786copy number variation1nstd204human GRCh38.p13 chr6: 33,016,601-33,499,100 , GRCh37.p13 chr6: 32,984,378-33,466,877 COL11A2, RXRB, 39 more genes
    nsv5231680copy number variation1nstd204human GRCh38.p13 chr6: 33,147,343-33,172,499 , GRCh37.p13 chr6: 33,115,120-33,140,276 HCG24, COL11A2
    nsv5221500copy number variation1nstd204human GRCh38.p13 chr6: 33,159,059-33,164,099 , GRCh37.p13 chr6: 33,126,836-33,131,876 COL11A2
    nsv4934591copy number variation1nstd200human GRCh38 chr6: 33,146,377-33,172,258 , GRCh37.p13 chr6: 33,114,154-33,140,035 COL11A2, HCG24
    nsv4828618copy number variation1nstd200human GRCh37 chr6: 33,114,154-33,140,035 , GRCh38.p12 chr6: 33,146,377-33,172,258 HCG24, COL11A2
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4682849copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,141,458-33,419,703 , GRCh38.p12 chr6: 33,173,681-33,451,926 RPL35AP4, RGL2, 29 more genes
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4656065copy number variation1nstd186human GRCh37 chr6: 33,128,974-33,129,031 , GRCh38.p12 chr6: 33,161,197-33,161,254 COL11A2
    nsv4578633copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,131,455-33,139,880 , GRCh38.p12 chr6: 33,163,678-33,172,103 COL11A2
    nsv4451881copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,131,435-33,419,703 , GRCh38 chr6: 33,163,658-33,451,926 COL11A2, HSD17B8, 29 more genes
    nsv4392323copy number variation1nstd171human GRCh37 chr6: 33,128,974-33,129,031 , GRCh38.p12 chr6: 33,161,197-33,161,254 COL11A2
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 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