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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097331copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,162,409-44,154,249 , GRCh38.p12 chr6: 42,194,671-44,186,512 MRPS10, CUL9, 70 more genes
    nsv6791704copy number variation1nstd229human GRCh38 chr6: 42,737,001-44,115,000 , GRCh37.p13 chr6: 42,704,739-44,082,737 ZNF318, RPL24P4, 56 more genes
    nsv6789524copy number variation1nstd229human GRCh38 chr6: 43,982,781-44,004,333 , GRCh37.p13 chr6: 43,950,518-43,972,070 SCIRT, LINC03040
    nsv6783044copy number variation1nstd229human GRCh38 chr6: 43,796,111-44,061,887 , GRCh37.p13 chr6: 43,763,848-44,029,624 LINC03040, LOC105375069, 5 more genes
    nsv6636332copy number variation1nstd102humanUncertain significance GRCh37 chr6: 43,571,555-44,154,599 , GRCh38.p12 chr6: 43,603,818-44,186,862 CAPN11, LOC105375068, 18 more genes
    nsv6566770inversion1nstd223human GRCh38 chr6: 42,194,666-44,186,502 , GRCh37.p13 chr6: 42,162,404-44,154,239 RPL36AP5, MIR6780B, 70 more genes
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6301968copy number variation1nstd186human GRCh37 chr6: 43,972,781-43,972,855 , GRCh38.p12 chr6: 44,005,044-44,005,118 LINC03040, SCIRT
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6135515copy number variation1nstd213human GRCh37 chr6: 43,220,000-44,970,001 , GRCh38.p12 chr6: 43,252,262-45,002,264 SLC29A1, NFKBIE, 54 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5470241copy number variation1nstd206human GRCh38 chr6: 44,005,044-44,005,118 , GRCh37.p13 chr6: 43,972,781-43,972,855 SCIRT, LINC03040
    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
    nsv3961106insertion1nstd168human GRCh38 chr6: 43,983,645-44,096,636 , GRCh37.p13 chr6: 43,951,382-44,064,373 LINC03040, RPL29P16, 1 more genes
    nsv3956708copy number variation1nstd168human GRCh38 chr6: 43,960,338-44,010,820 , GRCh37.p13 chr6: 43,928,075-43,978,557 LINC03040, SCIRT
    nsv3924318copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,336,296-44,558,281 , NCBI36 chr6: 42,444,274-44,666,259 , GRCh38 chr6: 42,368,558-44,590,544 MIR4642, SRF, 82 more genes
    nsv3919521copy number variation1nstd102humanPathogenic NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843 RPL23P6, LOC102723789, 184 more genes
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