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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891559copy number variation1nstd209human GRCh38 chr6: 149,835,627-149,836,914 , GRCh37.p13 chr6: 150,156,763-150,158,050 LRP11
    nsv5889600copy number variation1nstd209human GRCh38 chr6: 149,837,359-149,838,195 , GRCh37.p13 chr6: 150,158,495-150,159,331 LRP11
    nsv5844649copy number variation1nstd209human GRCh38 chr6: 149,835,578-149,836,977 , GRCh37.p13 chr6: 150,156,714-150,158,113 LRP11
    nsv5689880mobile element insertion1nstd211human GRCh38 chr6: 149,854,928-149,854,928 , GRCh37.p13 chr6: 150,176,064-150,176,064 LRP11
    nsv5457185copy number variation1nstd206human GRCh38 chr6: 149,817,634-149,817,722 , GRCh37.p13 chr6: 150,138,770-150,138,858 LRP11
    nsv5410760mobile element insertion1nstd206human GRCh38 chr6: 149,854,928-149,854,979 , GRCh37.p13 chr6: 150,176,064-150,176,115 LRP11
    nsv4675234copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929 RNU7-3P, HSPD1P16, 86 more genes
    nsv4608747copy number variation1nstd183human GRCh37 chr6: 150,183,543-150,184,488 , GRCh38.p12 chr6: 149,862,407-149,863,352 RAET1E-AS1, LRP11, 1 more genes
    nsv4606243copy number variation1nstd183human GRCh37 chr6: 150,140,272-150,144,473 , GRCh38.p12 chr6: 149,819,136-149,823,337 LRP11
    nsv4456488copy number variation1nstd102humanPathogenic GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222 PDCL3P5, SYTL3, 176 more genes
    nsv4436722copy number variation1nstd102humanPathogenic GRCh37 chr6: 148,690,764-150,494,873 , GRCh38.p12 chr6: 148,369,628-150,173,737 PCMT1, ULBP3, 42 more genes
    nsv4377133copy number variation1nstd173human GRCh37 chr6: 150,096,941-150,159,452 , GRCh38.p12 chr6: 149,775,805-149,838,316 LOC107986660, BTBD10P2, 2 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4150001copy number variation1nstd166human GRCh37.p13 chr6: 150,155,479-150,155,600 , GRCh38.p12 chr6: 149,834,343-149,834,464 LRP11
    nsv4146115copy number variation1nstd166human GRCh37.p13 chr6: 150,158,589-150,159,349 , GRCh38.p12 chr6: 149,837,453-149,838,213 LRP11
    nsv4145701copy number variation1nstd166human GRCh37.p13 chr6: 150,153,037-150,159,336 , GRCh38.p12 chr6: 149,831,901-149,838,200 LRP11
    nsv3957666copy number variation1nstd168human GRCh38 chr6: 149,834,621-149,861,120 , GRCh37.p13 chr6: 150,155,757-150,182,256 LRP11
    nsv3920975copy number variation1nstd102humanPathogenic GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591 UST-AS2, LOC729681, 394 more genes
    nsv3920651copy number variation1nstd102humanPathogenic GRCh38 chr6: 144,932,561-152,985,364 , NCBI36 chr6: 145,295,390-153,348,192 , GRCh37 chr6: 145,253,697-153,306,499 PPP1R14C, RAET1K, 107 more genes
    nsv3919153copy number variation1nstd102humanUncertain significance NCBI36 chr6: 147,943,180-150,590,792 , GRCh37 chr6: 147,901,487-150,549,099 , GRCh38 chr6: 147,580,351-150,227,963 PHB1P1, RAET1M, 45 more genes
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