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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6792601copy number variation1nstd229human GRCh38 chr6: 26,035,437-26,331,519 , GRCh37.p13 chr6: 26,035,665-26,331,747 TRS-AGA2-1, H2AC8, 49 more genes
    nsv6789669copy number variation1nstd229human GRCh38 chr6: 25,978,117-26,742,203 , GRCh37.p13 chr6: 25,978,345-26,585,842 H2AC8, BTN1A1P1, 93 more genes
    nsv6787290copy number variation1nstd229human GRCh38 chr6: 25,240,953-26,330,257 , GRCh37.p13 chr6: 25,241,181-26,330,485 CARMIL1, H2AC8, 74 more genes
    nsv6778997copy number variation1nstd229human GRCh38 chr6: 26,092,832-26,212,882 , GRCh37.p13 chr6: 26,093,060-26,213,110 RPS10P1, H1-12P, 14 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
    nsv6415562copy number variation1nstd223human GRCh38 chr6: 25,975,489-26,254,942 , GRCh37.p13 chr6: 25,975,717-26,255,170 H2AC7, H3P26, 38 more genes
    nsv6402318copy number variation1nstd223human GRCh38 chr6: 25,240,953-26,330,257 , GRCh37.p13 chr6: 25,241,181-26,330,485 H2BC7, H2AC7, 74 more genes
    nsv6401522copy number variation1nstd223human GRCh38 chr6: 26,102,415-26,260,224 , GRCh37.p13 chr6: 26,102,643-26,260,452 H2AC7, H4C7, 24 more genes
    nsv6400617copy number variation1nstd223human GRCh38 chr6: 26,092,832-26,212,879 , GRCh37.p13 chr6: 26,093,060-26,213,107 H2BC7, RPS10P1, 14 more genes
    nsv6290728copy number variation1nstd102humanPathogenic GRCh37 chr6: 26,008,259-26,168,230 , GRCh38.p12 chr6: 26,008,031-26,168,002 H2BC3, H1-1, 18 more genes
    nsv6290097copy number variation1nstd218human GRCh38.p12 chr6: 25,963,026-26,273,403 , GRCh37 chr6: 25,963,254-26,273,631 H1-2, H1-3, 41 more genes
    nsv6141014copy number variation1nstd206human GRCh38 chr6: 26,024,000-26,230,000 , GRCh37.p13 chr6: 26,024,228-26,230,228 H4C5, H2BC6, 26 more genes
    nsv5235046copy number variation1nstd204human GRCh38.p13 chr6: 26,155,101-26,158,961 , GRCh37.p13 chr6: 26,155,329-26,159,189 H2BC5, H1-4
    nsv5230906copy number variation1nstd204human GRCh38.p13 chr6: 26,154,001-26,161,000 , GRCh37.p13 chr6: 26,154,229-26,161,228 H1-4, H2BC5
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4934536copy number variation1nstd200human GRCh38 chr6: 26,150,781-26,331,570 , GRCh37.p13 chr6: 26,151,009-26,331,798 , LARP1P1, 41 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
    nsv4729341copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,046,566-26,670,193 , GRCh38.p12 chr6: 26,046,338-26,669,965 H1-4, TRV-CAC1-6, 78 more genes
    nsv4728787copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,090,243-26,265,667 , GRCh38.p12 chr6: 26,090,015-26,265,439 H2AC7, H2AC9P, 26 more genes
    nsv4598439copy number variation1nstd183human GRCh37 chr6: 26,153,284-26,235,966 , GRCh38.p12 chr6: 26,153,056-26,235,738 H1-3, H2BC7, 15 more genes
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