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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127711copy number variation1nstd186human GRCh37 chr18: 32,851,401-32,851,481 , GRCh38.p12 chr18: 35,271,437-35,271,517 ZSCAN30
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5705360mobile element insertion1nstd211human GRCh38 chr18: 35,273,386-35,273,386 , GRCh37.p13 chr18: 32,853,350-32,853,350 ZSCAN30
    nsv5562609sequence alteration1nstd206human GRCh38 chr18: 35,234,158-35,343,147 , GRCh37.p13 chr18: 32,814,122-32,923,111 , ZNF24, 3 more genes
    nsv5533194copy number variation1nstd206human GRCh38 chr18: 35,271,437-35,271,517 , GRCh37.p13 chr18: 32,851,401-32,851,481 ZSCAN30
    nsv5522459copy number variation1nstd206human GRCh38 chr18: 35,277,095-35,277,160 , GRCh37.p13 chr18: 32,857,059-32,857,124 ZSCAN30
    nsv5375166translocation1nstd200human GRCh38 chr18: 35,254,047-35,254,047 , GRCh38 chr18: 35,343,147-35,343,147 , GRCh37.p13 chr18: 32,923,111-32,923,111 , GRCh37.p13 chr18: 32,834,011-32,834,011 ZNF24, ZNF397, 1 more genes
    nsv5375165translocation1nstd200human GRCh38 chr18: 35,234,159-35,234,159 , GRCh38 chr18: 35,254,120-35,254,120 , GRCh37.p13 chr18: 32,814,123-32,814,123 , GRCh37.p13 chr18: 32,834,084-32,834,084 ZNF397, ZSCAN30
    nsv5340239translocation1nstd200human GRCh37 chr18: 32,923,111-32,923,111 , GRCh37 chr18: 32,834,011-32,834,011 , GRCh38.p12 chr18: 35,254,047-35,254,047 , GRCh38.p12 chr18: 35,343,147-35,343,147 ZNF24, ZNF397, 1 more genes
    nsv5323462copy number variation1nstd204human GRCh38.p13 chr18: 35,285,249-35,286,729 , GRCh37.p13 chr18: 32,865,213-32,866,693 ZSCAN30
    nsv5280700copy number variation1nstd204human GRCh38.p13 chr18: 35,285,301-35,286,700 , GRCh37.p13 chr18: 32,865,265-32,866,664 ZSCAN30
    nsv5150188mobile element insertion1nstd203human GRCh38 chr18: 35,273,370-35,273,386 , GRCh37.p13 chr18: 32,853,334-32,853,350 ZSCAN30
    nsv5036576inversion1nstd200human GRCh38 chr18: 33,011,377-36,071,277 , GRCh37.p13 chr18: 30,591,341-33,651,240 , ZSCAN30, 25 more genes
    nsv5024098copy number variation1nstd200human GRCh38 chr18: 35,262,029-35,279,067 , GRCh37.p13 chr18: 32,841,993-32,859,031 ZSCAN30
    nsv5011323copy number variation1nstd200human GRCh38 chr18: 35,285,254-35,286,726 , GRCh37.p13 chr18: 32,865,218-32,866,690 ZSCAN30
    nsv5011322copy number variation1nstd200human GRCh38 chr18: 35,277,095-35,277,160 , GRCh37.p13 chr18: 32,857,059-32,857,124 ZSCAN30
    nsv4871565inversion1nstd200human GRCh37 chr18: 30,591,341-33,651,241 , GRCh38.p12 chr18: 33,011,377-36,071,278 , LOC105372066, 25 more genes
    nsv4859250copy number variation1nstd200human GRCh37 chr18: 32,865,218-32,866,690 , GRCh38.p12 chr18: 35,285,254-35,286,726 ZSCAN30
    nsv4729854copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,971,647-33,737,300 , GRCh38.p12 chr18: 26,391,683-36,157,337 CLUHP6, KLHL14, 100 more genes
    nsv4709902inversion2nstd195human GRCh37 chr18: 32,868,918-32,868,919 , GRCh38.p12 chr18: 35,288,954-35,288,955 ZNF271P, ZSCAN30
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