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Items: 1 to 20 of 760

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5953888insertion1nstd209human GRCh38 chr2: 121,610,913-121,610,913 , GRCh37.p13 chr2: 122,368,489-122,368,489 CLASP1
    nsv5951902insertion1nstd209human GRCh38 chr2: 121,583,902-121,583,902 , GRCh37.p13 chr2: 122,341,478-122,341,478 CLASP1
    nsv5893801copy number variation1nstd209human GRCh38 chr2: 121,531,382-121,531,979 , GRCh37.p13 chr2: 122,288,958-122,289,555 CLASP1, RNU4ATAC, 1 more genes
    nsv5891950copy number variation1nstd209human GRCh38 chr2: 121,334,594-121,336,122 , GRCh37.p13 chr2: 122,092,170-122,093,698 CLASP1
    nsv5891150copy number variation1nstd209human GRCh38 chr2: 121,557,385-121,558,046 , GRCh37.p13 chr2: 122,314,961-122,315,622 CLASP1
    nsv5890441copy number variation1nstd209human GRCh38 chr2: 121,384,019-121,384,144 , GRCh37.p13 chr2: 122,141,595-122,141,720 CLASP1
    nsv5890002copy number variation1nstd209human GRCh38 chr2: 121,399,999-121,400,136 , GRCh37.p13 chr2: 122,157,575-122,157,712 CLASP1
    nsv5831126copy number variation1nstd209human GRCh38 chr2: 121,334,566-121,336,465 , GRCh37.p13 chr2: 122,092,142-122,094,041 CLASP1
    nsv5722311mobile element insertion1nstd211human GRCh38 chr2: 121,590,626-121,590,626 , GRCh37.p13 chr2: 122,348,202-122,348,202 CLASP1
    nsv5717583mobile element insertion1nstd211human GRCh38 chr2: 121,609,270-121,609,270 , GRCh37.p13 chr2: 122,366,846-122,366,846 CLASP1
    nsv5690874mobile element insertion1nstd211human GRCh38 chr2: 121,458,550-121,458,550 , GRCh37.p13 chr2: 122,216,126-122,216,126 CLASP1
    nsv5690481mobile element insertion1nstd211human GRCh38 chr2: 121,460,705-121,460,705 , GRCh37.p13 chr2: 122,218,281-122,218,281 CLASP1
    nsv5688693mobile element insertion1nstd211human GRCh38 chr2: 121,488,759-121,488,759 , GRCh37.p13 chr2: 122,246,335-122,246,335 CLASP1
    nsv5687349mobile element insertion2nstd211human GRCh38 chr2: 121,341,872-121,341,872 , GRCh37.p13 chr2: 122,099,448-122,099,448 CLASP1
    nsv5679125mobile element insertion1nstd211human GRCh38 chr2: 121,478,720-121,478,720 , GRCh37.p13 chr2: 122,236,296-122,236,296 CLASP1
    nsv5678690mobile element insertion2nstd211human GRCh38 chr2: 121,583,914-121,583,914 , GRCh37.p13 chr2: 122,341,490-122,341,490 CLASP1
    nsv5678231mobile element insertion1nstd211human GRCh38 chr2: 121,508,060-121,508,060 , GRCh37.p13 chr2: 122,265,636-122,265,636 CLASP1
    nsv5610705insertion1nstd207human GRCh38 chr2: 121,611,600-121,611,600 , GRCh37.p13 chr2: 122,369,176-122,369,176 CLASP1
    nsv5609294insertion1nstd207human GRCh38 chr2: 121,583,902-121,583,902 , GRCh37.p13 chr2: 122,341,478-122,341,478 CLASP1
    nsv5568786copy number variation1nstd207human GRCh38 chr2: 121,334,594-121,336,122 , GRCh37.p13 chr2: 122,092,170-122,093,698 CLASP1
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