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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950999insertion1nstd209human GRCh38 chr5: 149,370,028-149,370,028 , GRCh37.p13 chr5: 148,749,591-148,749,591 PCYOX1L
    nsv5634188insertion1nstd207human GRCh38 chr5: 149,370,033-149,370,033 , GRCh37.p13 chr5: 148,749,596-148,749,596 PCYOX1L
    nsv5552999insertion1nstd206human GRCh38 chr5: 149,370,028-149,370,061 , GRCh37.p13 chr5: 148,749,591-148,749,624 PCYOX1L
    nsv5097677mobile element insertion1nstd203human GRCh38 chr5: 149,370,024-149,370,061 , GRCh37.p13 chr5: 148,749,587-148,749,624 PCYOX1L
    nsv5097029mobile element insertion1nstd203human GRCh38 chr5: 149,370,019-149,370,067 , GRCh37.p13 chr5: 148,749,582-148,749,630 PCYOX1L
    nsv5095017mobile element insertion1nstd203human GRCh38 chr5: 149,370,027-149,370,061 , GRCh37.p13 chr5: 148,749,590-148,749,624 PCYOX1L
    nsv5094064mobile element insertion1nstd203human GRCh38 chr5: 149,370,028-149,370,061 , GRCh37.p13 chr5: 148,749,591-148,749,624 PCYOX1L
    nsv5093616mobile element insertion1nstd203human GRCh38 chr5: 149,370,025-149,370,067 , GRCh37.p13 chr5: 148,749,588-148,749,630 PCYOX1L
    nsv5091303mobile element insertion1nstd203human GRCh38 chr5: 149,370,022-149,370,061 , GRCh37.p13 chr5: 148,749,585-148,749,624 PCYOX1L
    nsv5089269mobile element insertion1nstd203human GRCh38 chr5: 149,372,710-149,372,727 , GRCh37.p13 chr5: 148,752,273-148,752,290 PCYOX1L, IL17B
    nsv5088850mobile element insertion1nstd203human GRCh38 chr5: 149,370,026-149,370,061 , GRCh37.p13 chr5: 148,749,589-148,749,624 PCYOX1L
    nsv5088304mobile element insertion1nstd203human GRCh38 chr5: 149,370,023-149,370,061 , GRCh37.p13 chr5: 148,749,586-148,749,624 PCYOX1L
    nsv5085886mobile element insertion1nstd203human GRCh38 chr5: 149,370,034-149,370,061 , GRCh37.p13 chr5: 148,749,597-148,749,624 PCYOX1L
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4939139copy number variation1nstd200human GRCh38 chr5: 149,369,532-149,375,449 , GRCh37.p13 chr5: 148,749,095-148,755,012 PCYOX1L, IL17B
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4814922copy number variation1nstd200human GRCh37 chr5: 148,749,095-148,755,012 , GRCh38.p12 chr5: 149,369,532-149,375,449 PCYOX1L, IL17B
    nsv4765508insertion1nstd199human GRCh37 chr5: 148,749,589-148,749,589 , GRCh38.p12 chr5: 149,370,026-149,370,026 PCYOX1L
    nsv4723830insertion1nstd186human GRCh37 chr5: 148,749,591-148,749,591 , GRCh38.p12 chr5: 149,370,028-149,370,028 PCYOX1L
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