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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7041334inversion1nstd229human GRCh38 chr6: 29,474,330-30,422,378 , GRCh37.p13 chr6: 29,442,107-30,390,155 HCG4, HLA-F, 80 more genes
    nsv6794544copy number variation1nstd229human GRCh38 chr6: 29,648,159-29,659,738 , GRCh37.p13 chr6: 29,615,936-29,627,515 MOG
    nsv6788069copy number variation1nstd229human GRCh38 chr6: 29,662,960-29,666,534 , GRCh37.p13 chr6: 29,630,737-29,634,311 MOG
    nsv6782341copy number variation1nstd229human GRCh38 chr6: 29,672,027-29,676,894 , GRCh37.p13 chr6: 29,639,804-29,644,671 MOG, ZFP57
    nsv6782296copy number variation1nstd229human GRCh38 chr6: 29,500,962-29,679,645 , GRCh37.p13 chr6: 29,468,739-29,647,422 RPL13AP, LINC01015, 12 more genes
    nsv6636314copy number variation1nstd102humanUncertain significance GRCh37 chr6: 29,162,783-30,236,331 , GRCh38.p12 chr6: 29,195,006-30,268,554 LOC353009, OR2H2, 92 more genes
    nsv6573551inversion1nstd223human GRCh38 chr6: 29,665,407-29,665,879 , GRCh37.p13 chr6: 29,633,184-29,633,656 MOG
    nsv6569554inversion1nstd223human GRCh38 chr6: 29,665,407-29,665,801 , GRCh37.p13 chr6: 29,633,184-29,633,578 MOG
    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
    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
    nsv5969880inversion1nstd209human GRCh38 chr6: 29,665,581-29,665,728 , GRCh37.p13 chr6: 29,633,358-29,633,505 MOG
    nsv5845121copy number variation1nstd209human GRCh38 chr6: 29,656,780-29,657,811 , GRCh37.p13 chr6: 29,624,557-29,625,588 MOG
    nsv5562335sequence alteration1nstd206human GRCh38 chr6: 29,665,311-29,665,779 , GRCh37.p13 chr6: 29,633,088-29,633,556 MOG
    nsv5466176copy number variation1nstd206human GRCh38 chr6: 29,668,065-29,668,159 , GRCh37.p13 chr6: 29,635,842-29,635,936 MOG
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4949402copy number variation1nstd200human GRCh38 chr6: 29,672,143-29,674,111 , GRCh37.p13 chr6: 29,639,920-29,641,888 ZFP57, MOG
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4828574copy number variation1nstd200human GRCh37 chr6: 29,639,920-29,641,888 , GRCh38.p12 chr6: 29,672,143-29,674,111 MOG, ZFP57
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