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Items: 1 to 20 of 135

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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
    nsv7045629inversion1nstd229human GRCh38 chr6: 30,007,594-31,355,527 , GRCh37.p13 chr6: 29,975,371-31,323,304 USP8P1, LINC02571, 82 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
    nsv6784630copy number variation1nstd229human GRCh38 chr6: 30,262,744-30,262,817 , GRCh37.p13 chr6: 30,230,521-30,230,594 HCG17, HLA-L
    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
    nsv6562568inversion1nstd223human GRCh38 chr6: 29,766,029-31,471,345 , GRCh37.p13 chr6: 29,733,806-31,439,122 HCG4P9, LINC01149, 126 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
    nsv6267939copy number variation1nstd214human GRCh38 chr6: 30,262,742-30,262,813 , GRCh37.p13 chr6: 30,230,519-30,230,590 HCG17, HLA-L
    nsv6135917copy number variation1nstd213human GRCh37 chr6: 30,110,000-32,450,001 , GRCh38.p12 chr6: 30,142,223-32,482,224 ABCF1, AGER, 186 more genes
    nsv6015698copy number variation1nstd212human GRCh38 chr6: 30,262,742-30,262,814 , GRCh37.p13 chr6: 30,230,519-30,230,591 HLA-L, HCG17
    nsv5576525copy number variation1nstd207human GRCh38 chr6: 30,262,742-30,262,813 , GRCh37.p13 chr6: 30,230,519-30,230,590 HLA-L, HCG17
    nsv5387169copy number variation1nstd186human GRCh37 chr6: 30,230,521-30,230,591 , GRCh38.p12 chr6: 30,262,744-30,262,814 HCG17, HLA-L
    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
    nsv4940637copy number variation1nstd200human GRCh38 chr6: 30,262,816-30,262,914 , GRCh37.p13 chr6: 30,230,593-30,230,691 HLA-L, HCG17
    nsv4815806copy number variation1nstd200human GRCh37 chr6: 30,230,521-30,230,591 , GRCh38.p12 chr6: 30,262,744-30,262,814 HLA-L, HCG17
    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
    nsv4651080copy number variation1nstd186human GRCh37 chr6: 30,230,520-30,230,591 , GRCh38.p12 chr6: 30,262,743-30,262,814 HLA-L, HCG17
    nsv4394142copy number variation1nstd174human GRCh37 chr6: 30,230,519-30,230,591 , GRCh38.p12 chr6: 30,262,742-30,262,814 HCG17, HLA-L
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