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Items: 1 to 20 of 344

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141388copy number variation1nstd232human GRCh37.p13 chr19: 11,107,054-11,107,166 , GRCh38.p12 chr19: 10,996,378-10,996,490 SMARCA4
    nsv7095460copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,105,494-11,172,492 , GRCh38.p12 chr19: 10,994,818-11,061,816 RN7SL192P, SMARCA4
    nsv7095459copy number variation1nstd102humanPathogenic GRCh37 chr19: 11,098,332-11,105,687 , GRCh38.p12 chr19: 10,987,656-10,995,011 SMARCA4
    nsv7095458copy number variation4nstd102humanUncertain significance GRCh37 chr19: 10,828,919-13,482,613 , GRCh38.p12 chr19: 10,718,243-13,371,799 WDR83OS, RPL10P16, 140 more genes
    nsv7095261copy number variation1nstd102humanPathogenic GRCh37 chr19: 11,121,047-11,136,194 , GRCh38.p12 chr19: 11,010,371-11,025,518 SMARCA4, RN7SL192P
    nsv7095183copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 11,168,921-11,169,575 , GRCh38.p12 chr19: 11,058,245-11,058,899 SMARCA4
    nsv7095182copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,134,174-11,144,896 , GRCh38.p12 chr19: 11,023,498-11,034,220 SMARCA4
    nsv7095181copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,129,613-11,172,492 , GRCh38.p12 chr19: 11,018,937-11,061,816 SMARCA4
    nsv7095180copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,113,695-11,172,492 , GRCh38.p12 chr19: 11,003,019-11,061,816 SMARCA4, RN7SL192P
    nsv7071346inversion1nstd229human GRCh38 chr19: 11,017,913-11,018,033 , GRCh37.p13 chr19: 11,128,589-11,128,709 SMARCA4
    nsv7069851inversion1nstd229human GRCh38 chr19: 11,059,106-11,073,641 , GRCh37.p13 chr19: 11,169,782-11,184,317 SMARCA4
    nsv7061047inversion1nstd229human GRCh38 chr19: 10,123,796-11,885,300 , GRCh37.p13 chr19: 10,234,472-11,996,115 QTRT1, ZNF653, 82 more genes
    nsv7059861inversion1nstd229human GRCh38 chr19: 10,970,652-10,972,884 , GRCh37.p13 chr19: 11,081,328-11,083,560 SMARCA4
    nsv7017619copy number variation1nstd229human GRCh38 chr19: 10,948,257-10,959,090 , GRCh37.p13 chr19: 11,058,933-11,069,766 SMARCA4
    nsv7017341copy number variation1nstd229human GRCh38 chr19: 10,985,382-10,985,796 , GRCh37.p13 chr19: 11,096,058-11,096,472 SMARCA4
    nsv7016236copy number variation1nstd229human GRCh38 chr19: 10,962,955-10,968,075 , GRCh37.p13 chr19: 11,073,631-11,078,751 SMARCA4
    nsv7014532copy number variation1nstd229human GRCh38 chr19: 11,047,443-11,048,231 , GRCh37.p13 chr19: 11,158,119-11,158,907 SMARCA4
    nsv7013636copy number variation1nstd229human GRCh38 chr19: 10,969,701-10,972,900 , GRCh37.p13 chr19: 11,080,377-11,083,576 SMARCA4
    nsv7011627copy number variation1nstd229human GRCh38 chr19: 11,027,951-11,030,731 , GRCh37.p13 chr19: 11,138,627-11,141,407 SMARCA4
    nsv7008303copy number variation1nstd229human GRCh38 chr19: 10,973,852-10,981,035 , GRCh37.p13 chr19: 11,084,528-11,091,711 SMARCA4
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