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Items: 1 to 20 of 226

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968207inversion1nstd209human GRCh38 chr3: 46,053,712-46,427,427 , GRCh37.p13 chr3: 46,095,204-46,468,918 CCR1, CCR3, 9 more genes
    nsv5957886insertion1nstd209human GRCh38 chr3: 46,243,005-46,243,005 , GRCh37.p13 chr3: 46,284,496-46,284,496 CCR3
    nsv5691313mobile element insertion1nstd211human GRCh38 chr3: 46,226,202-46,226,202 , GRCh37.p13 chr3: 46,267,693-46,267,693 CCR3
    nsv5691256mobile element insertion1nstd211human GRCh38 chr3: 46,213,101-46,213,101 , GRCh37.p13 chr3: 46,254,592-46,254,592 CCR3
    nsv5622960insertion1nstd207human GRCh38 chr3: 46,242,982-46,242,982 , GRCh37.p13 chr3: 46,284,473-46,284,473 CCR3
    nsv5563336sequence alteration1nstd206human GRCh38 chr3: 46,053,233-46,427,907 , GRCh37.p13 chr3: 46,094,725-46,469,398 CCR1, UQCRC2P1, 9 more genes
    nsv5451679copy number variation1nstd206human GRCh38 chr3: 46,267,191-46,269,126 , GRCh37.p13 chr3: 46,308,682-46,310,617 CCR3
    nsv5446112copy number variation1nstd206human GRCh38 chr3: 46,246,506-46,251,846 , GRCh37.p13 chr3: 46,287,997-46,293,337 CCR3
    nsv5445043copy number variation1nstd206human GRCh38 chr3: 46,253,912-46,253,968 , GRCh37.p13 chr3: 46,295,403-46,295,459 CCR3
    nsv5437466copy number variation1nstd206human GRCh38 chr3: 46,257,186-46,257,264 , GRCh37.p13 chr3: 46,298,677-46,298,755 CCR3
    nsv5407149mobile element insertion1nstd206human GRCh38 chr3: 46,226,202-46,226,253 , GRCh37.p13 chr3: 46,267,693-46,267,744 CCR3
    nsv5396018mobile element insertion1nstd206human GRCh38 chr3: 46,213,101-46,213,152 , GRCh37.p13 chr3: 46,254,592-46,254,643 CCR3
    nsv5351732translocation1nstd200human GRCh38 chr3: 46,259,446-46,259,446 , GRCh38 chr3: 46,259,374-46,259,374 , GRCh37.p13 chr3: 46,300,865-46,300,865 , GRCh37.p13 chr3: 46,300,937-46,300,937 CCR3
    nsv5351731translocation1nstd200human GRCh38 chr3: 46,257,264-46,257,264 , GRCh38 chr3: 46,257,186-46,257,186 , GRCh37.p13 chr3: 46,298,677-46,298,677 , GRCh37.p13 chr3: 46,298,755-46,298,755 CCR3
    nsv5060178mobile element insertion1nstd203human GRCh38 chr3: 46,261,001-46,261,019 , GRCh37.p13 chr3: 46,302,492-46,302,510 CCR3
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924388copy number variation1nstd200human GRCh38 chr3: 46,244,401-46,246,439 , GRCh37.p13 chr3: 46,285,892-46,287,930 CCR3
    nsv4911112copy number variation1nstd200human GRCh38 chr3: 46,244,780-46,246,703 , GRCh37.p13 chr3: 46,286,271-46,288,194 CCR3
    nsv4911111copy number variation1nstd200human GRCh38 chr3: 46,231,122-46,232,969 , GRCh37.p13 chr3: 46,272,613-46,274,460 CCR3
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