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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978684insertion1nstd209human GRCh38 chr19: 41,119,665-41,119,665 , GRCh37.p13 chr19: 41,625,570-41,625,570 CYP2F1
    nsv5977639inversion1nstd209human GRCh38 chr19: 40,827,499-41,120,720 , GRCh37.p13 chr19: 41,333,404-41,626,625 , CYP2A6, 8 more genes
    nsv5564058sequence alteration1nstd206human GRCh38 chr19: 40,827,060-41,121,102 , GRCh37.p13 chr19: 41,332,965-41,627,007 , CYP2F2P, 9 more genes
    nsv5520346copy number variation1nstd206human GRCh38 chr19: 41,119,346-41,148,853 , GRCh37.p13 chr19: 41,625,251-41,654,758 CYP2F1, CYP2T3P
    nsv5375442translocation1nstd200human GRCh38 chr19: 40,827,501-40,827,501 , GRCh38 chr19: 41,120,721-41,120,721 , GRCh37.p13 chr19: 41,333,406-41,333,406 , GRCh37.p13 chr19: 41,626,626-41,626,626 CYP2F1
    nsv5375441translocation1nstd200human GRCh38 chr19: 40,823,681-40,823,681 , GRCh38 chr19: 41,122,636-41,122,636 , GRCh37.p13 chr19: 41,628,541-41,628,541 , GRCh37.p13 chr19: 41,329,586-41,329,586 CYP2F1, CYP2F2P
    nsv5343212translocation1nstd200human GRCh37 chr19: 41,333,406-41,333,406 , GRCh37 chr19: 41,626,626-41,626,626 , GRCh38.p12 chr19: 41,120,721-41,120,721 , GRCh38.p12 chr19: 40,827,501-40,827,501 CYP2F1
    nsv5331094translocation1nstd200human GRCh37 chr19: 41,628,541-41,628,541 , GRCh37 chr19: 41,329,586-41,329,586 , GRCh38.p12 chr19: 40,823,681-40,823,681 , GRCh38.p12 chr19: 41,122,636-41,122,636 CYP2F1, CYP2F2P
    nsv5328215translocation1nstd204human GRCh38.p13 chr19: 40,827,501-40,827,501 , GRCh38.p13 chr19: 41,120,721-41,120,721 , GRCh37.p13 chr19: 41,333,406-41,333,406 , GRCh37.p13 chr19: 41,626,626-41,626,626 CYP2F1
    nsv5020467copy number variation1nstd200human GRCh38 chr19: 41,118,165-41,120,169 , GRCh37.p13 chr19: 41,624,070-41,626,074 CYP2F1
    nsv4865176copy number variation1nstd200human GRCh37 chr19: 41,632,163-41,676,484 , GRCh38.p12 chr19: 41,126,258-41,170,579 RPL36P16, CYP2F1, 1 more genes
    nsv4727923copy number variation1nstd197human GRCh38.p12 chr19: 41,121,958-41,122,133 , GRCh37 chr19: 41,627,863-41,628,038 CYP2F1
    nsv4676245copy number variation1nstd102humanUncertain significance GRCh37 chr19: 41,304,025-41,928,997 , GRCh38.p12 chr19: 40,798,120-41,423,092 CYP2T1P, RN7SL34P, 26 more genes
    nsv4623167copy number variation1nstd183human GRCh37 chr19: 41,516,401-41,644,274 , GRCh38.p12 chr19: 41,010,496-41,138,369 CYP2A7P1, CYP2A13, 4 more genes
    nsv4622290copy number variation2nstd183human GRCh37 chr19: 41,626,703-41,628,623 , GRCh38.p12 chr19: 41,120,798-41,122,718 CYP2F1
    nsv4618758copy number variation1nstd183human GRCh37 chr19: 41,627,318-41,627,507 , GRCh38.p12 chr19: 41,121,413-41,121,602 CYP2F1
    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
    nsv4342305sequence alteration1nstd166human GRCh37.p13 chr19: 41,333,004-41,626,979 , GRCh38.p12 chr19: 40,827,099-41,121,074 , CYP2A7P1, 9 more genes
    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
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
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