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Items: 1 to 20 of 113

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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
    nsv7050769inversion1nstd229human GRCh38 chr6: 27,131,516-27,134,911 , GRCh37.p13 chr6: 27,099,295-27,102,690 H2BC11, H2AC11
    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
    nsv6563406inversion1nstd223human GRCh38 chr6: 25,888,425-29,704,317 , GRCh37.p13 chr6: 25,888,653-29,672,094 OR1F12P, H4C2, 362 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
    nsv5473084copy number variation1nstd206human GRCh38 chr6: 27,132,731-27,133,715 , GRCh37.p13 chr6: 27,100,510-27,101,494 H2BC11, H2AC11
    nsv5233032copy number variation1nstd204human GRCh38.p13 chr6: 27,132,956-27,135,464 , GRCh37.p13 chr6: 27,100,735-27,103,243 H2BC11, H2AC11
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4940503copy number variation1nstd200human GRCh38 chr6: 27,133,231-27,133,383 , GRCh37.p13 chr6: 27,101,010-27,101,162 H2AC11, H2BC11
    nsv4940502copy number variation1nstd200human GRCh38 chr6: 27,132,141-27,134,626 , GRCh37.p13 chr6: 27,099,920-27,102,405 H2BC11, H2AC11
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4815706copy number variation1nstd200human GRCh37 chr6: 27,099,920-27,102,405 , GRCh38.p12 chr6: 27,132,141-27,134,626 H2AC11, H2BC11
    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
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