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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054546inversion1nstd229human GRCh38 chr6: 27,132,770-27,436,246 , GRCh37.p13 chr6: 27,100,549-27,404,025 H4C9, TRQ-CTG5-1, 35 more genes
    nsv7051905inversion1nstd229human GRCh38 chr6: 27,014,906-27,279,038 , GRCh37.p13 chr6: 26,982,685-27,246,817 TRV-CAC6-1, CDCA7P1, 30 more genes
    nsv7051852inversion1nstd229human GRCh38 chr6: 27,083,111-27,189,507 , GRCh37.p13 chr6: 27,050,890-27,157,286 H2AC12, TRI-AAT5-2, 12 more genes
    nsv7044265inversion1nstd229human GRCh38 chr6: 27,145,490-27,145,579 , GRCh37.p13 chr6: 27,113,269-27,113,358 H2BC12, H2AC12
    nsv6794883copy number variation1nstd229human GRCh38 chr6: 27,143,641-27,144,302 , GRCh37.p13 chr6: 27,111,420-27,112,081 H2BC12
    nsv6779876copy number variation1nstd229human GRCh38 chr6: 27,083,896-27,138,638 , GRCh37.p13 chr6: 27,051,675-27,106,417 H2AC11, H2BC12, 6 more genes
    nsv6572221inversion1nstd223human GRCh38 chr6: 27,142,691-27,143,366 , GRCh37.p13 chr6: 27,110,470-27,111,145 H2BC12
    nsv6563406inversion1nstd223human GRCh38 chr6: 25,888,425-29,704,317 , GRCh37.p13 chr6: 25,888,653-29,672,094 OR1F12P, H4C2, 362 more genes
    nsv6140551copy number variation1nstd206human GRCh38 chr6: 27,146,588-27,147,536 , GRCh37.p13 chr6: 27,114,367-27,115,315 H2AC12, MIR3143, 1 more genes
    nsv6135506copy number variation1nstd213human GRCh37 chr6: 27,060,000-27,130,001 , GRCh38.p12 chr6: 27,092,221-27,162,222 H4C9, H2AC11, 10 more genes
    nsv5472571copy number variation1nstd206human GRCh38 chr6: 27,146,409-27,146,483 , GRCh37.p13 chr6: 27,114,188-27,114,262 H2AC12, MIR3143, 1 more genes
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 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
    nsv4592193copy number variation1nstd183human GRCh37 chr6: 27,099,872-27,115,362 , GRCh38.p12 chr6: 27,132,093-27,147,583 H4C9, H2AC11, 4 more genes
    nsv4381128copy number variation1nstd173human GRCh37 chr6: 26,941,502-27,391,254 , GRCh38.p12 chr6: 26,973,723-27,423,475 , RPL10P2, 45 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
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
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