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 174

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898363copy number variation1nstd209human GRCh38 chr6: 31,196,035-31,196,194 , GRCh37.p13 chr6: 31,163,812-31,163,971 HCG27
    nsv5895365copy number variation1nstd209human GRCh38 chr6: 31,196,540-31,196,641 , GRCh37.p13 chr6: 31,164,317-31,164,418 HCG27
    nsv5643027insertion1nstd207human GRCh38 chr6: 31,201,077-31,201,077 , GRCh37.p13 chr6: 31,168,854-31,168,854 HCG27
    nsv5473857copy number variation1nstd206human GRCh38 chr6: 31,196,071-31,196,151 , GRCh37.p13 chr6: 31,163,848-31,163,928 HCG27
    nsv5466381copy number variation1nstd206human GRCh38 chr6: 31,196,568-31,196,642 , GRCh37.p13 chr6: 31,164,345-31,164,419 HCG27
    nsv5466068copy number variation1nstd206human GRCh38 chr6: 31,193,814-31,199,194 , GRCh37.p13 chr6: 31,161,591-31,166,971 HCG27
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5117600mobile element insertion1nstd203human GRCh38 chr6: 31,197,234-31,197,241 , GRCh37.p13 chr6: 31,165,011-31,165,018 HCG27
    nsv4940665copy number variation1nstd200human GRCh38 chr6: 31,191,882-31,207,484 , GRCh37.p13 chr6: 31,159,659-31,175,261 HCG27
    nsv4828597copy number variation1nstd200human GRCh37 chr6: 31,163,063-31,163,563 , GRCh38.p12 chr6: 31,195,286-31,195,786 HCG27
    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
    nsv4716726mobile element insertion1nstd186human GRCh37 chr6: 31,168,854-31,168,854 , GRCh38.p12 chr6: 31,201,077-31,201,077 HCG27
    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
    nsv4646502copy number variation1nstd186human GRCh37 chr6: 31,131,451-31,272,307 , GRCh38.p12 chr6: 31,163,674-31,304,530 POU5F1, PSORS1C3, 8 more genes
    nsv4490485mobile element insertion1nstd166human GRCh37.p13 chr6: 31,168,854-31,168,854 , GRCh38.p12 chr6: 31,201,077-31,201,077 HCG27
    nsv4436473complex substitution1nstd102humanUncertain significance GRCh38.p12 chr6: 31,117,423-31,356,870 , GRCh37 chr6: 31,085,200-31,324,647 CDSN, HLA-B, 15 more genes
    nsv4403147copy number variation1nstd174human GRCh37 chr6: 30,372,579-31,314,243 , GRCh38.p12 chr6: 30,404,802-31,346,466 MIR4640, NAPGP2, 58 more genes
    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