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 137

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6794940copy number variation1nstd229human GRCh38 chr6: 28,477,067-28,753,900 , GRCh37.p13 chr6: 28,444,844-28,721,677 TRS-GCT4-1, TRMEP1, 28 more genes
    nsv6781884copy number variation1nstd229human GRCh38 chr6: 28,507,791-28,509,238 , GRCh37.p13 chr6: 28,475,568-28,477,015 GPX6
    nsv6778388copy number variation1nstd229human GRCh38 chr6: 28,446,401-28,556,000 , GRCh37.p13 chr6: 28,414,178-28,523,777 GPX6, TRT-TGT1-1, 10 more genes
    nsv6631147copy number variation1nstd224human GRCh37 chr6: 28,425,755-28,645,170 , GRCh38.p12 chr6: 28,457,978-28,677,393 GPX6, TRR-TCG5-1, 19 more genes
    nsv6631020copy number variation1nstd224human GRCh37 chr6: 28,414,166-28,647,984 , GRCh38.p12 chr6: 28,446,389-28,680,207 GPX5, OR2E1P, 21 more genes
    nsv6563406inversion1nstd223human GRCh38 chr6: 25,888,425-29,704,317 , GRCh37.p13 chr6: 25,888,653-29,672,094 OR1F12P, H4C2, 362 more genes
    nsv6289880copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 28,005,012-31,683,185 , GRCh38.p12 chr6: 28,037,234-31,715,408 ABCF1, AIF1, 313 more genes
    nsv6184897copy number variation1nstd214human GRCh38 chr6: 28,503,002-28,503,069 , GRCh37.p13 chr6: 28,470,779-28,470,846 GPX6
    nsv6135508copy number variation1nstd213human GRCh37 chr6: 27,710,000-30,110,001 , GRCh38.p12 chr6: 27,742,221-30,142,224 GABBR1, H1-5, 224 more genes
    nsv6014099copy number variation1nstd212human GRCh38 chr6: 28,502,468-28,502,547 , GRCh37.p13 chr6: 28,470,245-28,470,324 GPX6
    nsv5641293insertion1nstd207human GRCh38 chr6: 28,501,976-28,501,976 , GRCh37.p13 chr6: 28,469,753-28,469,753 GPX6
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 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
    nsv4378463copy number variation1nstd173human GRCh37 chr6: 28,409,344-28,523,625 , GRCh38.p12 chr6: 28,441,567-28,555,848 OR2E1P, TRMEP1, 11 more genes
    nsv4366948copy number variation1nstd173human GRCh37 chr6: 28,418,991-28,523,625 , GRCh38.p12 chr6: 28,451,214-28,555,848 TRL-AAG4-1, TRT-CGT1-1, 9 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3915580copy number variation1nstd102humanUncertain significance NCBI36 chr6: 28,516,623-28,779,629 , GRCh37.p13 chr6: 28,408,644-28,671,650 , GRCh38.p12 chr6: 28,440,867-28,703,873 SCAND3, TRK-TTT13-1, 24 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