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Items: 1 to 20 of 111

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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
    nsv6793062copy number variation1nstd229human GRCh38 chr6: 29,479,801-29,541,300 , GRCh37.p13 chr6: 29,447,578-29,509,077 RPS17P1, LOC105375008, 4 more genes
    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
    nsv6779338copy number variation1nstd229human GRCh38 chr6: 29,419,464-29,620,038 , GRCh37.p13 chr6: 29,387,241-29,587,815 GABBR1, RPL13AP, 19 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
    nsv6563406inversion1nstd223human GRCh38 chr6: 25,888,425-29,704,317 , GRCh37.p13 chr6: 25,888,653-29,672,094 OR1F12P, H4C2, 362 more genes
    nsv6411794copy number variation1nstd223human GRCh38 chr6: 29,502,709-29,574,025 , GRCh37.p13 chr6: 29,470,486-29,541,802 OR2H5P, OR2I1P, 4 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
    nsv5727879mobile element insertion1nstd211human GRCh38 chr6: 29,510,653-29,510,653 , GRCh37.p13 chr6: 29,478,430-29,478,430 LINC02829
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4949399copy number variation1nstd200human GRCh38 chr6: 29,502,709-29,574,025 , GRCh37.p13 chr6: 29,470,486-29,541,802 GPR53P, LINC01015, 4 more genes
    nsv4949398copy number variation1nstd200human GRCh38 chr6: 29,501,526-29,511,156 , GRCh37.p13 chr6: 29,469,303-29,478,933 LINC02829
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4828572copy number variation1nstd200human GRCh37 chr6: 29,469,303-29,478,933 , GRCh38.p12 chr6: 29,501,526-29,511,156 LINC02829
    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
    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
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