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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5897402copy number variation1nstd209human GRCh38 chr6: 43,630,692-43,632,970 , GRCh37.p13 chr6: 43,598,429-43,600,707 MAD2L1BP, GTPBP2
    nsv5844966copy number variation1nstd209human GRCh38 chr6: 43,630,692-43,632,120 , GRCh37.p13 chr6: 43,598,429-43,599,857 MAD2L1BP, GTPBP2
    nsv5844908copy number variation1nstd209human GRCh38 chr6: 43,630,992-43,633,020 , GRCh37.p13 chr6: 43,598,729-43,600,757 GTPBP2, MAD2L1BP
    nsv5673766copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,928,506-43,737,486 , GRCh38.p12 chr6: 42,960,768-43,769,749 SRF, POLR1C, 39 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
    nsv5462518copy number variation1nstd206human GRCh38 chr6: 43,630,652-43,633,044 , GRCh37.p13 chr6: 43,598,389-43,600,781 MAD2L1BP, GTPBP2
    nsv5362902translocation1nstd200human GRCh38 chr6: 43,632,153-43,632,153 , GRCh38 chr6: 43,631,764-43,631,764 , GRCh37.p13 chr6: 43,599,501-43,599,501 , GRCh37.p13 chr6: 43,599,890-43,599,890 GTPBP2, MAD2L1BP
    nsv4941155copy number variation1nstd200human GRCh38 chr6: 43,637,209-43,637,311 , GRCh37.p13 chr6: 43,604,946-43,605,048 MAD2L1BP
    nsv4816208copy number variation1nstd200human GRCh37 chr6: 43,605,573-43,606,004 , GRCh38.p12 chr6: 43,637,836-43,638,267 MAD2L1BP
    nsv4816207copy number variation1nstd200human GRCh37 chr6: 43,599,501-43,599,891 , GRCh38.p12 chr6: 43,631,764-43,632,154 MAD2L1BP, GTPBP2
    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
    nsv4665476copy number variation1nstd186human GRCh37 chr6: 43,598,329-43,600,642 , GRCh38.p12 chr6: 43,630,592-43,632,905 GTPBP2, MAD2L1BP
    nsv4592687copy number variation1nstd183human GRCh37 chr6: 43,598,329-43,600,642 , GRCh38.p12 chr6: 43,630,592-43,632,905 MAD2L1BP, GTPBP2
    nsv4592655copy number variation1nstd183human GRCh37 chr6: 43,596,320-43,597,609 , GRCh38.p12 chr6: 43,628,583-43,629,872 MAD2L1BP, GTPBP2
    nsv4410932copy number variation1nstd174human GRCh37 chr6: 43,598,329-43,600,755 , GRCh38.p12 chr6: 43,630,592-43,633,018 GTPBP2, MAD2L1BP
    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
    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
    nsv3922186copy number variation1nstd102humanUncertain significance NCBI36 chr6: 43,613,072-43,860,167 , GRCh38 chr6: 43,537,357-43,784,452 , GRCh37 chr6: 43,505,094-43,752,189 MRPS18A, GTPBP2, 8 more genes
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