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Items: 1 to 20 of 226

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068631inversion1nstd229human GRCh38 chr18: 35,241,317-35,304,305 , GRCh37.p13 chr18: 32,821,281-32,884,269 ZNF271P, ZNF397, 1 more genes
    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
    nsv7007521copy number variation1nstd229human GRCh38 chr18: 35,256,201-35,289,300 , GRCh37.p13 chr18: 32,836,165-32,869,264 ZSCAN30, ZNF397, 1 more genes
    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
    nsv5714127mobile element insertion1nstd211human GRCh38 chr18: 35,292,760-35,292,760 , GRCh37.p13 chr18: 32,872,724-32,872,724 ZNF271P
    nsv5562609sequence alteration1nstd206human GRCh38 chr18: 35,234,158-35,343,147 , GRCh37.p13 chr18: 32,814,122-32,923,111 , ZNF24, 3 more genes
    nsv5522330copy number variation1nstd206human GRCh38 chr18: 35,294,782-35,306,768 , GRCh37.p13 chr18: 32,874,746-32,886,732 ZNF271P
    nsv5427529mobile element insertion1nstd206human GRCh38 chr18: 35,292,760-35,292,811 , GRCh37.p13 chr18: 32,872,724-32,872,775 ZNF271P
    nsv5347247translocation1nstd200human GRCh38 chr7: 78,325,842-78,325,842 , GRCh38 chr18: 35,307,103-35,307,103 , GRCh37.p13 chr18: 32,887,067-32,887,067 , GRCh37.p13 chr7: 77,955,159-77,955,159 ZNF271P, MAGI2
    nsv5036576inversion1nstd200human GRCh38 chr18: 33,011,377-36,071,277 , GRCh37.p13 chr18: 30,591,341-33,651,240 , ZSCAN30, 25 more genes
    nsv5011325copy number variation1nstd200human GRCh38 chr18: 35,295,703-35,295,771 , GRCh37.p13 chr18: 32,875,667-32,875,735 ZNF271P
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