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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147818insertion1nstd232human GRCh37.p13 chr6: 30,029,796-30,029,796 , GRCh38.p12 chr6: 30,062,019-30,062,019 POLR1H
    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
    nsv6779786copy number variation1nstd229human GRCh38 chr6: 30,060,362-30,069,713 , GRCh37.p13 chr6: 30,028,139-30,037,490 PPP1R11, RNF39, 2 more genes
    nsv6636358copy number variation1nstd102humanUncertain significance GRCh37 chr6: 29,730,504-30,202,199 , GRCh38.p12 chr6: 29,762,727-30,234,422 HCG4P8, HLA-V, 45 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
    nsv6562568inversion1nstd223human GRCh38 chr6: 29,766,029-31,471,345 , GRCh37.p13 chr6: 29,733,806-31,439,122 HCG4P9, LINC01149, 126 more genes
    nsv6411845copy number variation1nstd223human GRCh38 chr6: 29,881,401-30,173,300 , GRCh37.p13 chr6: 29,849,178-30,141,077 RNF39, ETF1P1, 28 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
    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
    nsv4728011copy number variation2nstd197human GRCh38.p12 chr6: 29,723,465-30,109,048 , GRCh37 chr6: 29,691,242-30,076,825 HLA-A, HLA-F, 45 more genes
    nsv4598473copy number variation1nstd183human GRCh37 chr6: 30,028,889-30,035,672 , GRCh38.p12 chr6: 30,061,112-30,067,895 POLR1H, POLR1HASP, 1 more genes
    nsv4436385complex substitution1nstd102humanUncertain significance GRCh38.p12 chr6: 29,942,601-30,108,066 , GRCh37 chr6: 29,910,378-30,075,843 HLA-A, HLA-J, 15 more genes
    nsv4375146copy number variation1nstd173human GRCh37 chr6: 30,021,127-30,067,087 , GRCh38.p12 chr6: 30,053,350-30,099,310 PPP1R11, POLR1H, 2 more genes
    nsv4372231copy number variation1nstd173human GRCh37 chr6: 30,030,189-30,061,262 , GRCh38.p12 chr6: 30,062,412-30,093,485 RNF39, PPP1R11, 1 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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