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Items: 1 to 20 of 134

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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
    nsv6790569copy number variation1nstd229human GRCh38 chr6: 30,325,461-30,326,008 , GRCh37.p13 chr6: 30,293,238-30,293,785 TRIM39, HCG17, 1 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
    nsv6413811copy number variation1nstd223human GRCh38 chr6: 30,326,301-30,328,100 , GRCh37.p13 chr6: 30,294,078-30,295,877 HCG17, TRIM39, 2 more genes
    nsv6308676insertion1nstd186human GRCh37 chr6: 30,303,328-30,303,367 , GRCh38.p12 chr6: 30,335,551-30,335,590 TRIM39, TRIM39-RPP21
    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
    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
    nsv5535702insertion1nstd206human GRCh38 chr6: 30,335,551-30,335,590 , GRCh37.p13 chr6: 30,303,328-30,303,367 TRIM39-RPP21, TRIM39
    nsv5459452copy number variation1nstd206human GRCh38 chr6: 30,334,322-30,334,929 , GRCh37.p13 chr6: 30,302,099-30,302,706 TRIM39-RPP21, TRIM39
    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
    nsv5105932mobile element insertion1nstd203human GRCh38 chr6: 30,335,539-30,335,551 , GRCh37.p13 chr6: 30,303,316-30,303,328 TRIM39, TRIM39-RPP21
    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
    nsv4387194copy number variation1nstd173human GRCh37 chr6: 30,127,521-30,311,296 , GRCh38.p12 chr6: 30,159,744-30,343,519 HLA-L, TRIM39-RPP21, 9 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
    nsv3969984copy number variation1nstd168human GRCh38 chr6: 30,182,174-30,347,083 , GRCh37.p13 chr6: 30,149,951-30,314,860 HLA-L, TRIM26, 7 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
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