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Items: 1 to 20 of 949

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145394copy number variation1nstd232human GRCh37.p13 chr6: 676,132-676,236 , GRCh38.p12 chr6: 676,132-676,236 EXOC2
    nsv7144261copy number variation1nstd232human GRCh37.p13 chr6: 676,783-676,837 , GRCh38.p12 chr6: 676,783-676,837 EXOC2
    nsv7141722copy number variation1nstd232human GRCh37.p13 chr6: 675,587-675,637 , GRCh38.p12 chr6: 675,587-675,637 EXOC2
    nsv7141363copy number variation1nstd232human GRCh37.p13 chr6: 676,336-676,496 , GRCh38.p12 chr6: 676,336-676,496 EXOC2
    nsv7138050copy number variation1nstd232human GRCh37.p13 chr6: 675,519-675,679 , GRCh38.p12 chr6: 675,519-675,679 EXOC2
    nsv7137073copy number variation1nstd102humanPathogenic GRCh37 chr6: 491,126-1,624,775 , GRCh38.p12 chr6: 491,126-1,624,540 RN7SL352P, LOC107986555, 18 more genes
    nsv7137049copy number variation1nstd102humanPathogenic GRCh37 chr6: 393,153-3,751,765 , GRCh38.p12 chr6: 393,153-3,751,531 LOC105374883, LINC02525, 57 more genes
    nsv7093358copy number variation1nstd102humanUncertain significance GRCh37 chr6: 160,000-820,000 , GRCh38.p12 chr6: 160,000-820,000 EXOC2, LOC105374873, 7 more genes
    nsv7053844inversion1nstd229human GRCh38 chr6: 673,422-673,486 , GRCh37.p13 chr6: 673,422-673,486 EXOC2
    nsv7053643inversion1nstd229human GRCh38 chr6: 588,446-761,055 , GRCh37.p13 chr6: 588,446-761,055 LOC105374873, MARK2P18, 2 more genes
    nsv7053468inversion1nstd229human GRCh38 chr6: 285,653-485,550 , GRCh37.p13 chr6: 285,653-485,550 EXOC2, DUSP22, 1 more genes
    nsv7050648inversion1nstd229human GRCh38 chr6: 669,745-672,380 , GRCh37.p13 chr6: 669,745-672,380 MARK2P18, EXOC2
    nsv7046172inversion1nstd229human GRCh38 chr6: 661,174-670,060 , GRCh37.p13 chr6: 661,174-670,060 MARK2P18, EXOC2
    nsv7044518inversion1nstd229human GRCh38 chr6: 608,246-894,067 , GRCh37.p13 chr6: 608,246-894,068 MARK2P18, LOC105374873, 3 more genes
    nsv7038102inversion1nstd229human GRCh38 chr6: 425,843-695,237 , GRCh37.p13 chr6: 425,843-695,237 HUS1B, MARK2P18, 1 more genes
    nsv6797880copy number variation1nstd229human GRCh38 chr6: 469,822-499,966 , GRCh37.p13 chr6: 469,822-499,966 EXOC2
    nsv6797693copy number variation1nstd229human GRCh38 chr6: 573,618-586,470 , GRCh37.p13 chr6: 573,618-586,470 EXOC2
    nsv6797676copy number variation1nstd229human GRCh38 chr6: 524,001-532,000 , GRCh37.p13 chr6: 524,001-532,000 EXOC2
    nsv6796430copy number variation1nstd229human GRCh38 chr6: 632,346-632,406 , GRCh37.p13 chr6: 632,346-632,406 EXOC2
    nsv6795296copy number variation1nstd229human GRCh38 chr6: 660,353-665,625 , GRCh37.p13 chr6: 660,353-665,625 EXOC2
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