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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965107insertion1nstd209human GRCh38 chr5: 134,856,324-134,856,324 , GRCh37.p13 chr5: 134,192,014-134,192,014 C5orf24
    nsv5688301mobile element insertion1nstd211human GRCh38 chr5: 134,853,551-134,853,551 , GRCh37.p13 chr5: 134,189,241-134,189,241 C5orf24
    nsv5685004mobile element insertion2nstd211human GRCh38 chr5: 134,856,339-134,856,339 , GRCh37.p13 chr5: 134,192,029-134,192,029 C5orf24
    nsv5678245mobile element insertion1nstd211human GRCh38 chr5: 134,845,755-134,845,755 , GRCh37.p13 chr5: 134,181,445-134,181,445 C5orf24
    nsv5642289insertion1nstd207human GRCh38 chr5: 134,856,324-134,856,324 , GRCh37.p13 chr5: 134,192,014-134,192,014 C5orf24
    nsv5464745copy number variation1nstd206human GRCh38 chr5: 134,848,359-134,848,704 , GRCh37.p13 chr5: 134,184,049-134,184,394 C5orf24
    nsv5408209mobile element insertion1nstd206human GRCh38 chr5: 134,856,339-134,856,387 , GRCh37.p13 chr5: 134,192,029-134,192,077 C5orf24
    nsv5394204mobile element insertion1nstd206human GRCh38 chr5: 134,845,755-134,845,806 , GRCh37.p13 chr5: 134,181,445-134,181,496 C5orf24
    nsv5237330copy number variation1nstd204human GRCh38.p13 chr5: 134,843,160-134,883,337 , GRCh37.p13 chr5: 134,178,850-134,219,027 C5orf24, TXNDC15
    nsv5235021copy number variation1nstd204human GRCh38.p13 chr5: 134,841,301-134,885,000 , GRCh37.p13 chr5: 134,176,991-134,220,690 TXNDC15, C5orf24
    nsv5222689copy number variation1nstd204human GRCh38.p13 chr5: 134,562,401-134,881,200 , GRCh37.p13 chr5: 133,898,091-134,216,890 SAR1B, RNU6-1311P, 9 more genes
    nsv5100022mobile element insertion1nstd203human GRCh38 chr5: 134,856,328-134,856,337 , GRCh37.p13 chr5: 134,192,018-134,192,027 C5orf24
    nsv5092977mobile element insertion1nstd203human GRCh38 chr5: 134,856,329-134,856,339 , GRCh37.p13 chr5: 134,192,019-134,192,029 C5orf24
    nsv5080442mobile element insertion1nstd203human GRCh38 chr5: 134,848,645-134,848,658 , GRCh37.p13 chr5: 134,184,335-134,184,348 C5orf24
    nsv5080168mobile element insertion1nstd203human GRCh38 chr5: 134,856,324-134,856,339 , GRCh37.p13 chr5: 134,192,014-134,192,029 C5orf24
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 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
    nsv4938698copy number variation1nstd200human GRCh38 chr5: 134,839,688-134,839,778 , GRCh37.p13 chr5: 134,175,378-134,175,468 C5orf24
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
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