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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5951606copy number variation1nstd209human GRCh38 chr20: 63,257,204-63,257,463 , GRCh37.p13 chr20: 61,888,556-61,888,815 FLJ16779
    nsv5949729copy number variation1nstd209human GRCh38 chr20: 63,257,338-63,257,857 , GRCh37.p13 chr20: 61,888,690-61,889,209 FLJ16779
    nsv5559866sequence alteration1nstd206human GRCh38 chr20: 62,865,770-63,725,218 , GRCh37.p13 chr20: 61,497,122-62,356,570 , PTK6, 46 more genes
    nsv5526398copy number variation1nstd206human GRCh38 chr20: 63,257,281-63,257,881 , GRCh37.p13 chr20: 61,888,633-61,889,233 FLJ16779
    nsv5517411copy number variation1nstd206human GRCh38 chr20: 63,261,644-63,267,573 , GRCh37.p13 chr20: 61,892,996-61,898,925 FLJ16779
    nsv5381809copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,510,452-62,315,381 , GRCh38.p12 chr20: 62,879,100-63,684,028 MIR3196, NKAIN4, 40 more genes
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5338574translocation1nstd200human GRCh37 chr20: 61,888,749-61,888,749 , GRCh37 chr20: 61,889,160-61,889,160 , GRCh38.p12 chr20: 63,257,397-63,257,397 , GRCh38.p12 chr20: 63,257,808-63,257,808 FLJ16779
    nsv5293467copy number variation1nstd204human GRCh38.p13 chr20: 62,966,101-64,149,200 , GRCh37.p13 chr20: 61,597,453-62,780,553 , ZGPAT, 72 more genes
    nsv5291430copy number variation1nstd204human GRCh37.p13 chr20: 61,880,653-61,973,852 , GRCh38.p13 chr20: 63,249,301-63,342,500 CHRNA4, ARFGAP1, 5 more genes
    nsv5287878copy number variation1nstd204human GRCh38.p13 chr20: 63,068,801-63,693,400 , GRCh37.p13 chr20: 61,700,153-62,324,753 , BIRC7, 33 more genes
    nsv4730030copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,884,113-62,234,685 , GRCh38.p12 chr20: 63,252,761-63,603,332 LOC105372725, ARFGAP1, 19 more genes
    nsv4729754copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,507,440-62,318,983 , GRCh38.p12 chr20: 62,876,088-63,687,630 DIDO1, LOC102723814, 41 more genes
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 more genes
    nsv4676208copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,152,321-62,915,555 , GRCh38.p12 chr20: 62,555,114-64,284,202 GMEB2, LOC105372727, 94 more genes
    nsv4676181copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052 LOC105372697, MIR647, 174 more genes
    nsv4457810copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,946,209-61,975,606 , GRCh38.p12 chr20: 62,371,153-63,344,254 SLCO4A1-AS2, ARFGAP1, 51 more genes
    nsv4457442copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,678,415-62,247,462 , GRCh38.p12 chr20: 63,047,063-63,616,109 LOC105376996, LOC105372725, 29 more genes
    nsv4436326complex substitution1nstd102humanUncertain significance GRCh37 chr20: 60,885,242-61,929,348 , GRCh38.p12 chr20: 62,310,186-63,297,996 COL9A3, LAMA5, 52 more genes
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