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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069366inversion1nstd229human GRCh38 chr18: 35,342,241-35,342,285 , GRCh37.p13 chr18: 32,922,205-32,922,249 ZNF24
    nsv7066164inversion1nstd229human GRCh38 chr18: 35,254,047-35,343,150 , GRCh37.p13 chr18: 32,834,011-32,923,114 ZNF271P, ZNF24, 2 more genes
    nsv7009519copy number variation1nstd229human GRCh38 chr18: 35,234,201-35,343,200 , GRCh37.p13 chr18: 32,814,165-32,923,164 ZNF271P, ZNF24, 2 more genes
    nsv7009293copy number variation1nstd229human GRCh38 chr18: 34,453,177-37,158,337 , GRCh37.p13 chr18: 32,033,141-34,738,300 LOC105372061, RNU4-3P, 31 more genes
    nsv7007040copy number variation1nstd229human GRCh38 chr18: 35,331,630-35,331,883 , GRCh37.p13 chr18: 32,911,594-32,911,847 ZNF24
    nsv6583218inversion1nstd223human GRCh38 chr18: 35,254,047-35,343,147 , GRCh37.p13 chr18: 32,834,011-32,923,111 ZNF24, ZNF271P, 2 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6133439copy number variation1nstd213human GRCh37 chr18: 28,680,000-49,600,001 , GRCh38.p12 chr18: 31,100,037-52,073,631 ATP5F1A, DSC1, 240 more genes
    nsv6133334copy number variation1nstd213human GRCh37 chr18: 32,810,000-34,010,001 , GRCh38.p12 chr18: 35,230,036-36,430,038 GALNT1, ZNF24, 23 more genes
    nsv6133333copy number variation1nstd213human GRCh37 chr18: 27,400,000-52,060,001 , GRCh38.p12 chr18: 29,820,035-54,532,766 ATP5F1A, DCC, 259 more genes
    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
    nsv6107779inversion1nstd212human GRCh38 chr18: 34,743,532-36,146,243 , GRCh37.p13 chr18: 32,323,496-33,726,206 , DTNA, 22 more genes
    nsv5562609sequence alteration1nstd206human GRCh38 chr18: 35,234,158-35,343,147 , GRCh37.p13 chr18: 32,814,122-32,923,111 , ZNF24, 3 more genes
    nsv5522994copy number variation1nstd206human GRCh38 chr18: 35,331,630-35,331,883 , GRCh37.p13 chr18: 32,911,594-32,911,847 , ZNF24
    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
    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
    nsv5291743copy number variation1nstd204human GRCh38.p13 chr18: 35,344,401-35,350,400 , GRCh37.p13 chr18: 32,924,365-32,930,364 ZNF24
    nsv5036576inversion1nstd200human GRCh38 chr18: 33,011,377-36,071,277 , GRCh37.p13 chr18: 30,591,341-33,651,240 , ZSCAN30, 25 more genes
    nsv4871565inversion1nstd200human GRCh37 chr18: 30,591,341-33,651,241 , GRCh38.p12 chr18: 33,011,377-36,071,278 , LOC105372066, 25 more genes
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