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Items: 1 to 20 of 948

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv5961571insertion1nstd209human GRCh38 chr4: 20,517,480-20,517,480 , GRCh37.p13 chr4: 20,519,103-20,519,103 SLIT2
    nsv5958489insertion1nstd209human GRCh38 chr4: 20,472,209-20,472,209 , GRCh37.p13 chr4: 20,473,832-20,473,832 SLIT2
    nsv5952330insertion1nstd209human GRCh38 chr4: 20,472,628-20,472,628 , GRCh37.p13 chr4: 20,474,251-20,474,251 SLIT2
    nsv5899211copy number variation1nstd209human GRCh38 chr4: 20,405,915-20,406,903 , GRCh37.p13 chr4: 20,407,538-20,408,526 SLIT2
    nsv5899025copy number variation1nstd209human GRCh38 chr4: 20,554,992-20,563,301 , GRCh37.p13 chr4: 20,556,615-20,564,924 SLIT2
    nsv5897783copy number variation1nstd209human GRCh38 chr4: 20,433,993-20,437,260 , GRCh37.p13 chr4: 20,435,616-20,438,883 SLIT2
    nsv5896982copy number variation1nstd209human GRCh38 chr4: 20,593,999-20,594,141 , GRCh37.p13 chr4: 20,595,622-20,595,764 SLIT2
    nsv5896235copy number variation1nstd209human GRCh38 chr4: 20,472,346-20,472,600 , GRCh37.p13 chr4: 20,473,969-20,474,223 SLIT2
    nsv5894251copy number variation1nstd209human GRCh38 chr4: 20,473,129-20,473,247 , GRCh37.p13 chr4: 20,474,752-20,474,870 SLIT2
    nsv5891860copy number variation1nstd209human GRCh38 chr4: 20,472,247-20,472,638 , GRCh37.p13 chr4: 20,473,870-20,474,261 SLIT2
    nsv5890790copy number variation1nstd209human GRCh38 chr4: 20,555,014-20,564,399 , GRCh37.p13 chr4: 20,556,637-20,566,022 SLIT2
    nsv5888021copy number variation1nstd209human GRCh38 chr4: 20,262,072-20,262,157 , GRCh37.p13 chr4: 20,263,695-20,263,780 SLIT2
    nsv5839222copy number variation1nstd209human GRCh38 chr4: 20,405,925-20,406,924 , GRCh37.p13 chr4: 20,407,548-20,408,547 SLIT2
    nsv5838894copy number variation1nstd209human GRCh38 chr4: 20,555,010-20,563,284 , GRCh37.p13 chr4: 20,556,633-20,564,907 SLIT2
    nsv5838633copy number variation1nstd209human GRCh38 chr4: 20,433,973-20,437,397 , GRCh37.p13 chr4: 20,435,596-20,439,020 SLIT2
    nsv5725014mobile element insertion2nstd211human GRCh38 chr4: 20,448,250-20,448,250 , GRCh37.p13 chr4: 20,449,873-20,449,873 SLIT2
    nsv5691481mobile element insertion1nstd211human GRCh38 chr4: 20,524,000-20,524,000 , GRCh37.p13 chr4: 20,525,623-20,525,623 SLIT2
    nsv5683035mobile element insertion2nstd211human GRCh38 chr4: 20,546,886-20,546,886 , GRCh37.p13 chr4: 20,548,509-20,548,509 SLIT2
    nsv5681915mobile element insertion2nstd211human GRCh38 chr4: 20,517,494-20,517,494 , GRCh37.p13 chr4: 20,519,117-20,519,117 SLIT2
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