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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940525copy number variation1nstd209human GRCh38 chr19: 40,399,855-40,399,904 , GRCh37.p13 chr19: 40,905,762-40,905,811 PRX
    nsv5648343insertion1nstd207human GRCh38 chr19: 40,406,273-40,406,273 , GRCh37.p13 chr19: 40,912,180-40,912,180 PRX
    nsv5596900copy number variation1nstd207human GRCh38 chr19: 40,399,855-40,399,904 , GRCh37.p13 chr19: 40,905,762-40,905,811 PRX
    nsv5558751sequence alteration1nstd206human GRCh38 chr19: 40,405,456-40,406,277 , GRCh37.p13 chr19: 40,911,363-40,912,184 PRX
    nsv5549146insertion1nstd206human GRCh38 chr19: 40,406,264-40,406,264 , GRCh37.p13 chr19: 40,912,171-40,912,171 PRX
    nsv5531513copy number variation1nstd206human GRCh38 chr19: 40,409,605-40,409,920 , GRCh37.p13 chr19: 40,915,512-40,915,827 PRX
    nsv5381266copy number variation1nstd102humanUncertain significance GRCh37 chr19: 40,902,613-40,902,614 , GRCh38 chr19: 40,396,706-40,396,707 PRX
    nsv5364903translocation1nstd200human GRCh38 chr19: 40,393,768-40,393,768 , GRCh38 chr10: 45,306,959-45,306,959 , GRCh37.p13 chr19: 40,899,675-40,899,675 , GRCh37.p13 chr10: 45,802,407-45,802,407 PRX, OR13A1
    nsv5354398translocation1nstd200human GRCh38 chr19: 40,394,435-40,394,435 , GRCh38 chr10: 45,306,960-45,306,960 , GRCh37.p13 chr10: 45,802,408-45,802,408 , GRCh37.p13 chr19: 40,900,342-40,900,342 OR13A1, PRX
    nsv5287129copy number variation1nstd204human GRCh38.p13 chr19: 40,119,401-40,793,500 , GRCh37.p13 chr19: 40,625,308-41,299,405 CCNP, SHKBP1, 28 more genes
    nsv5160086mobile element insertion1nstd203human GRCh38 chr19: 40,402,370-40,402,386 , GRCh37.p13 chr19: 40,908,277-40,908,293 PRX
    nsv4745753copy number variation1nstd199human GRCh37 chr19: 40,905,758-40,905,812 , GRCh38.p12 chr19: 40,399,851-40,399,905 PRX
    nsv4715731copy number variation1nstd195human GRCh37 chr19: 40,908,111-40,908,112 , GRCh38.p12 chr19: 40,402,204-40,402,205 PRX
    nsv4683466copy number variation1nstd102humanPathogenic GRCh37 chr19: 40,909,603-40,909,779 , GRCh38.p12 chr19: 40,403,696-40,403,872 PRX
    nsv4681045copy number variation3nstd102humanUncertain significance GRCh38 chr19: 40,396,707-40,396,784 , GRCh37 chr19: 40,902,614-40,902,691 PRX
    nsv4631212copy number variation1nstd183human GRCh37 chr19: 40,751,410-40,915,936 , GRCh38.p12 chr19: 40,245,503-40,410,029 AKT2, PLD3, 7 more genes
    nsv4560652sequence alteration1nstd166human GRCh37.p13 chr19: 40,911,363-40,912,182 , GRCh38.p12 chr19: 40,405,456-40,406,275 PRX
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4454769copy number variation1nstd102humanUncertain significance GRCh38 chr19: 40,393,956-40,407,942 , GRCh37 chr19: 40,899,863-40,913,849 PRX
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
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