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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6635793copy number variation1nstd227human GRCh37 chr19: 27,763,440-29,138,698 , GRCh38.p12 chr19: 27,272,532-28,647,791 LINC00662, SLC25A1P5, 10 more genes
    nsv6624884copy number variation1nstd224human GRCh37 chr19: 27,828,664-28,893,779 , GRCh38.p12 chr19: 27,337,756-28,402,872 LINC00662, SLC25A1P5, 7 more genes
    nsv6624858copy number variation1nstd224human GRCh37 chr19: 27,983,651-28,832,269 , GRCh38.p12 chr19: 27,492,743-28,341,362 LINC00662, SLC25A1P5, 7 more genes
    nsv6624705copy number variation1nstd224human GRCh37 chr19: 27,759,740-28,893,779 , GRCh38.p12 chr19: 27,268,832-28,402,872 LINC00662, SLC25A1P5, 7 more genes
    nsv6624458copy number variation1nstd224human GRCh37 chr19: 28,028,452-28,674,550 , GRCh38.p12 chr19: 27,537,544-28,183,643 LINC00662, SLC25A1P5, 7 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6054363copy number variation1nstd212human GRCh38 chr19: 27,861,056-27,861,884 , GRCh37.p13 chr19: 28,351,964-28,352,792 LINC02987, LOC105372348
    nsv5359677translocation1nstd200human GRCh38 chr19: 27,962,104-27,962,104 , GRCh38 chr19: 27,857,725-27,857,725 , GRCh37.p13 chr19: 28,453,012-28,453,012 , GRCh37.p13 chr19: 28,348,633-28,348,633 LINC02987, LOC105372348
    nsv5326215copy number variation1nstd204human GRCh37.p13 chr19: 28,348,632-28,453,013 , GRCh38.p13 chr19: 27,857,724-27,962,105 LINC02987, LOC105372347, 1 more genes
    nsv5295751copy number variation1nstd204human GRCh38.p13 chr19: 27,856,477-27,885,144 , GRCh37.p13 chr19: 28,347,385-28,376,052 LOC105372347, LINC02987, 1 more genes
    nsv5292230copy number variation1nstd204human GRCh38.p13 chr19: 27,823,162-27,863,051 , GRCh37.p13 chr19: 28,314,070-28,353,959 LINC02987, LOC105372348
    nsv5024514copy number variation1nstd200human GRCh38 chr19: 27,860,391-27,861,847 , GRCh37.p13 chr19: 28,351,299-28,352,755 LINC02987, LOC105372348
    nsv5024449copy number variation1nstd200human GRCh38 chr19: 27,354,891-27,982,739 , GRCh37.p13 chr19: 27,845,799-28,473,647 SLC25A1P5, LINC00662, 7 more genes
    nsv5020135copy number variation1nstd200human GRCh38 chr19: 27,852,216-27,854,822 , GRCh37.p13 chr19: 28,343,124-28,345,730 LOC105372348, LINC02987
    nsv5020033copy number variation1nstd200human GRCh38 chr19: 27,418,283-28,319,573 , GRCh37.p13 chr19: 27,909,191-28,810,480 , LOC105372348, 8 more genes
    nsv4865082copy number variation1nstd200human GRCh37 chr19: 27,845,799-28,473,647 , GRCh38.p12 chr19: 27,354,891-27,982,739 LINC00662, SLC25A1P5, 7 more genes
    nsv4861108copy number variation1nstd200human GRCh37 chr19: 28,351,841-28,353,192 , GRCh38.p12 chr19: 27,860,933-27,862,284 LINC02987, LOC105372348
    nsv4861107copy number variation1nstd200human GRCh37 chr19: 28,348,633-28,453,012 , GRCh38.p12 chr19: 27,857,725-27,962,104 LOC105372348, LOC105372347, 1 more genes
    nsv4708278copy number variation1nstd195human GRCh37 chr19: 28,353,401-28,355,851 , GRCh38.p12 chr19: 27,862,493-27,864,943 LINC02987, LOC105372348
    nsv4706401copy number variation1nstd195human GRCh37 chr19: 28,311,701-28,343,601 , GRCh38.p12 chr19: 27,820,793-27,852,693 LINC02987, LOC105372348
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