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Items: 1 to 20 of 129

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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
    nsv5559866sequence alteration1nstd206human GRCh38 chr20: 62,865,770-63,725,218 , GRCh37.p13 chr20: 61,497,122-62,356,570 , PTK6, 46 more genes
    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
    nsv5322110copy number variation1nstd204human GRCh38.p13 chr20: 63,177,398-63,177,793 , GRCh37.p13 chr20: 61,808,750-61,809,145 MIR124-3
    nsv5297002copy number variation1nstd204human GRCh38.p13 chr20: 63,174,401-63,180,100 , GRCh37.p13 chr20: 61,805,753-61,811,452 MIR124-3
    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
    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
    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
    nsv4625084copy number variation1nstd183human GRCh37 chr20: 61,809,647-61,809,970 , GRCh38.p12 chr20: 63,178,295-63,178,618 MIR124-3
    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
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv3966904insertion1nstd168human GRCh37.p13 chr20: 61,660,072-61,817,890 , GRCh38 chr20: 63,028,720-63,186,538 LINC01749, MIR124-3, 6 more genes
    nsv3924546copy number variation1nstd102humanLikely benign NCBI36 chr20: 61,040,937-61,300,767 , GRCh38 chr20: 62,939,140-63,198,970 , GRCh37 chr20: 61,570,492-61,830,322 YTHDF1, LOC105372718, 11 more genes
    nsv3924353copy number variation1nstd102humanPathogenic NCBI36 chr20: 59,335,000-62,379,123 , GRCh38 chr20: 61,326,549-64,277,326 , GRCh37 chr20: 59,901,605-62,908,679 PPDPF, CRMA, 126 more genes
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