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Items: 1 to 20 of 188

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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
    nsv6102004insertion1nstd212human GRCh38 chr19: 27,792,746-27,792,746 , GRCh37.p13 chr19: 28,283,654-28,283,654 LINC02987, LINC00662
    nsv5944196copy number variation1nstd209human GRCh38 chr19: 27,788,843-27,790,300 , GRCh37.p13 chr19: 28,279,751-28,281,208 LINC00662
    nsv5884951copy number variation1nstd209human GRCh38 chr19: 27,788,887-27,790,084 , GRCh37.p13 chr19: 28,279,795-28,280,992 LINC00662
    nsv5710722mobile element insertion1nstd211human GRCh38 chr19: 27,792,759-27,792,759 , GRCh37.p13 chr19: 28,283,667-28,283,667 LINC00662, LINC02987
    nsv5167807mobile element insertion1nstd203human GRCh38 chr19: 27,792,745-27,792,759 , GRCh37.p13 chr19: 28,283,653-28,283,667 LINC02987, LINC00662
    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
    nsv5020129copy number variation1nstd200human GRCh38 chr19: 27,788,024-27,793,838 , GRCh37.p13 chr19: 28,278,932-28,284,746 LINC00662, 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
    nsv4710599copy number variation1nstd195human GRCh37 chr19: 28,137,151-28,310,201 , GRCh38.p12 chr19: 27,646,243-27,819,293 LINC00662, SLC25A1P5, 3 more genes
    nsv4679383copy number variation1nstd189human GRCh37.p13 chr19: 27,951,818-28,895,255 , GRCh38.p12 chr19: 27,460,910-28,404,348 , LINC00662, 8 more genes
    nsv4679212copy number variation1nstd189human GRCh37.p13 chr19: 27,796,313-28,763,147 , GRCh38.p12 chr19: 27,305,405-28,272,240 LINC00662, SLC25A1P5, 7 more genes
    nsv4676123copy number variation1nstd102humanLikely benign GRCh37 chr19: 28,271,146-28,837,574 , GRCh38.p12 chr19: 27,780,238-28,346,667 LOC105372346, LINC02987, 6 more genes
    nsv4659592copy number variation1nstd186human GRCh37 chr19: 28,246,833-28,474,547 , GRCh38.p12 chr19: 27,755,925-27,983,639 LINC00662, SLC25A1P5, 6 more genes
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