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Items: 1 to 20 of 438

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970025inversion1nstd209human GRCh38 chr1: 51,313,199-51,545,140 , GRCh37.p13 chr1: 51,778,871-52,010,812 , EPS15, 6 more genes
    nsv5948625insertion1nstd209human GRCh38 chr1: 51,509,246-51,509,246 , GRCh37.p13 chr1: 51,974,918-51,974,918 EPS15
    nsv5887195copy number variation1nstd209human GRCh38 chr1: 51,395,237-51,395,391 , GRCh37.p13 chr1: 51,860,909-51,861,063 EPS15
    nsv5872811copy number variation1nstd209human GRCh38 chr1: 51,399,267-51,399,574 , GRCh37.p13 chr1: 51,864,939-51,865,246 EPS15
    nsv5872051copy number variation1nstd209human GRCh38 chr1: 51,449,479-51,451,782 , GRCh37.p13 chr1: 51,915,151-51,917,454 EPS15
    nsv5869056copy number variation1nstd209human GRCh38 chr1: 51,402,091-51,402,300 , GRCh37.p13 chr1: 51,867,763-51,867,972 EPS15
    nsv5830054copy number variation1nstd209human GRCh38 chr1: 51,449,432-51,451,806 , GRCh37.p13 chr1: 51,915,104-51,917,478 EPS15
    nsv5726825mobile element insertion2nstd211human GRCh38 chr1: 51,453,316-51,453,316 , GRCh37.p13 chr1: 51,918,988-51,918,988 EPS15
    nsv5692251mobile element insertion1nstd211human GRCh38 chr1: 51,457,510-51,457,510 , GRCh37.p13 chr1: 51,923,182-51,923,182 EPS15
    nsv5691198mobile element insertion1nstd211human GRCh38 chr1: 51,354,651-51,354,651 , GRCh37.p13 chr1: 51,820,323-51,820,323 EPS15
    nsv5679710mobile element insertion2nstd211human GRCh38 chr1: 51,509,257-51,509,257 , GRCh37.p13 chr1: 51,974,929-51,974,929 EPS15
    nsv5674335mobile element insertion2nstd211human GRCh38 chr1: 51,362,094-51,362,094 , GRCh37.p13 chr1: 51,827,766-51,827,766 EPS15
    nsv5610951insertion1nstd207human GRCh38 chr1: 51,504,974-51,504,974 , GRCh37.p13 chr1: 51,970,646-51,970,646 EPS15
    nsv5609271insertion1nstd207human GRCh38 chr1: 51,362,082-51,362,082 , GRCh37.p13 chr1: 51,827,754-51,827,754 EPS15
    nsv5605466insertion1nstd207human GRCh38 chr1: 51,509,246-51,509,246 , GRCh37.p13 chr1: 51,974,918-51,974,918 EPS15
    nsv5568907copy number variation1nstd207human GRCh38 chr1: 51,449,479-51,451,782 , GRCh37.p13 chr1: 51,915,151-51,917,454 EPS15
    nsv5562377sequence alteration1nstd206human GRCh38 chr1: 51,313,202-51,545,141 , GRCh37.p13 chr1: 51,778,874-52,010,813 , EPS15, 6 more genes
    nsv5433064copy number variation1nstd206human GRCh38 chr1: 51,357,368-51,357,445 , GRCh37.p13 chr1: 51,823,040-51,823,117 EPS15
    nsv5433025copy number variation1nstd206human GRCh38 chr1: 51,485,945-51,501,353 , GRCh37.p13 chr1: 51,951,617-51,967,025 EPS15
    nsv5429450copy number variation1nstd206human GRCh38 chr1: 51,359,971-51,360,083 , GRCh37.p13 chr1: 51,825,643-51,825,755 EPS15
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