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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940025copy number variation1nstd209human GRCh38 chr17: 75,905,217-75,905,326 , GRCh37.p13 chr17: 73,901,298-73,901,407 MRPL38
    nsv5375011translocation1nstd200human GRCh38 chr17: 75,903,251-75,903,251 , GRCh38 chr17: 75,903,699-75,903,699 , GRCh37.p13 chr17: 73,899,332-73,899,332 , GRCh37.p13 chr17: 73,899,780-73,899,780 MRPL38
    nsv5328292copy number variation1nstd204human GRCh37.p13 chr17: 73,892,370-73,903,784 , GRCh38.p13 chr17: 75,896,289-75,907,703 MRPL38, FBF1, 1 more genes
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5293100copy number variation1nstd204human GRCh38.p13 chr17: 75,896,301-75,907,600 , GRCh37.p13 chr17: 73,892,382-73,903,681 MRPL38, FBF1, 1 more genes
    nsv5288794copy number variation1nstd204human GRCh38.p13 chr17: 75,896,137-75,907,475 , GRCh37.p13 chr17: 73,892,218-73,903,556 TRIM65, MRPL38
    nsv5282727copy number variation1nstd204human GRCh38.p13 chr17: 75,896,112-75,903,562 , GRCh37.p13 chr17: 73,892,193-73,899,643 TRIM65, MRPL38
    nsv5282319copy number variation1nstd204human GRCh38.p13 chr17: 75,609,901-75,917,300 , GRCh37.p13 chr17: 73,605,982-73,913,381 ITGB4, TRIM65, 15 more genes
    nsv5016718copy number variation1nstd200human GRCh38 chr17: 75,896,291-75,907,687 , GRCh37.p13 chr17: 73,892,372-73,903,768 FBF1, TRIM65, 1 more genes
    nsv5016716copy number variation1nstd200human GRCh38 chr17: 75,883,689-75,922,191 , GRCh37.p13 chr17: 73,879,770-73,918,272 FBF1, TRIM65, 1 more genes
    nsv4858996copy number variation1nstd200human GRCh37 chr17: 73,892,364-73,903,785 , GRCh38.p12 chr17: 75,896,283-75,907,704 TRIM65, MRPL38, 1 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4499573mobile element insertion1nstd166human GRCh37.p13 chr17: 73,897,920-73,897,920 , GRCh38.p12 chr17: 75,901,839-75,901,839 MRPL38
    nsv4457679copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,596,063-73,959,466 , GRCh38.p12 chr17: 75,599,982-75,963,385 MIR4738, RECQL5, 16 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4365771copy number variation1nstd173human GRCh37 chr17: 73,820,227-73,895,909 , GRCh38.p12 chr17: 75,824,146-75,899,828 WBP2, TRIM47, 4 more genes
    nsv4336474sequence alteration1nstd166human GRCh37.p13 chr17: 73,898,780-73,899,781 , GRCh38.p12 chr17: 75,902,699-75,903,700 MRPL38
    nsv4269320copy number variation1nstd166human GRCh37.p13 chr17: 73,892,349-73,903,794 , GRCh38.p12 chr17: 75,896,268-75,907,713 FBF1, MRPL38, 1 more genes
    nsv3972399copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 64,159,738-74,891,024 , GRCh38.p12 chr17: 66,163,620-76,894,942 AANAT, ACOX1, 243 more genes
    nsv3963050copy number variation1nstd168human GRCh38 chr17: 75,874,585-75,900,629 , GRCh37.p13 chr17: 73,870,666-73,896,710 TRIM65, MRPL38, 1 more genes
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