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 106

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097331copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,162,409-44,154,249 , GRCh38.p12 chr6: 42,194,671-44,186,512 MRPS10, CUL9, 70 more genes
    nsv6791704copy number variation1nstd229human GRCh38 chr6: 42,737,001-44,115,000 , GRCh37.p13 chr6: 42,704,739-44,082,737 ZNF318, RPL24P4, 56 more genes
    nsv6784318copy number variation1nstd229human GRCh38 chr6: 43,802,277-43,870,123 , GRCh37.p13 chr6: 43,770,014-43,837,860 LOC105375068, LOC105375070, 2 more genes
    nsv6783044copy number variation1nstd229human GRCh38 chr6: 43,796,111-44,061,887 , GRCh37.p13 chr6: 43,763,848-44,029,624 LINC03040, LOC105375069, 5 more genes
    nsv6781548copy number variation1nstd229human GRCh38 chr6: 43,849,682-43,856,618 , GRCh37.p13 chr6: 43,817,419-43,824,355 LINC02537
    nsv6780925copy number variation1nstd229human GRCh38 chr6: 43,843,178-43,845,792 , GRCh37.p13 chr6: 43,810,915-43,813,529 LINC02537
    nsv6636332copy number variation1nstd102humanUncertain significance GRCh37 chr6: 43,571,555-44,154,599 , GRCh38.p12 chr6: 43,603,818-44,186,862 CAPN11, LOC105375068, 18 more genes
    nsv6566770inversion1nstd223human GRCh38 chr6: 42,194,666-44,186,502 , GRCh37.p13 chr6: 42,162,404-44,154,239 RPL36AP5, MIR6780B, 70 more genes
    nsv6405409copy number variation1nstd223human GRCh38 chr6: 43,845,423-43,847,695 , GRCh37.p13 chr6: 43,813,160-43,815,432 LINC02537
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6314599complex chromosomal rearrangement2nstd102humanUncertain significance GRCh38.p12 chr16: 65,792,466-65,792,466 , GRCh38.p12 chr16: 65,793,179-65,793,179 , GRCh37 chr16: 65,826,369-65,826,369 , GRCh37 chr16: 65,827,082-65,827,082 , GRCh38.p12 chr6: 43,843,609-43,843,609 , GRCh38.p12 chr6: 43,843,632-43,843,632 , GRCh37 chr6: 43,811,346-43,811,346 , GRCh37 chr6: 43,811,369-43,811,369 LINC02537
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6135515copy number variation1nstd213human GRCh37 chr6: 43,220,000-44,970,001 , GRCh38.p12 chr6: 43,252,262-45,002,264 SLC29A1, NFKBIE, 54 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv4941162copy number variation1nstd200human GRCh38 chr6: 43,802,277-43,870,121 , GRCh37.p13 chr6: 43,770,014-43,837,858 , LOC105375068, 3 more genes
    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
    nsv4497281mobile element insertion1nstd166human GRCh37.p13 chr6: 43,814,721-43,814,721 , GRCh38.p12 chr6: 43,846,984-43,846,984 , LINC02537
    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