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Items: 1 to 20 of 338

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137713insertion1nstd102humanUncertain significance GRCh37 chr18: 48,581,368-48,581,368 , GRCh38 chr18: 51,054,998-51,054,998 SMAD4
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5969313inversion1nstd209human GRCh38 chr18: 49,148,257-52,144,553 , GRCh37.p13 chr18: 46,674,627-49,670,923 , SMAD4, 52 more genes
    nsv5946010copy number variation1nstd209human GRCh38 chr18: 51,065,603-51,067,014 , GRCh37.p13 chr18: 48,591,973-48,593,384 SMAD4
    nsv5945807copy number variation1nstd209human GRCh38 chr18: 51,054,993-51,058,123 , GRCh37.p13 chr18: 48,581,363-48,584,493 SMAD4
    nsv5944928copy number variation1nstd209human GRCh38 chr18: 51,076,776-51,078,254 , GRCh37.p13 chr18: 48,603,146-48,604,624 SMAD4
    nsv5936736copy number variation1nstd209human GRCh38 chr18: 51,067,183-51,076,632 , GRCh37.p13 chr18: 48,593,553-48,603,002 SMAD4
    nsv5935605copy number variation1nstd209human GRCh38 chr18: 51,030,621-51,046,916 , GRCh37.p13 chr18: 48,556,991-48,573,286 , SMAD4
    nsv5934524copy number variation1nstd209human GRCh38 chr18: 51,058,244-51,058,338 , GRCh37.p13 chr18: 48,584,614-48,584,708 SMAD4
    nsv5929620copy number variation1nstd209human GRCh38 chr18: 51,047,293-51,048,682 , GRCh37.p13 chr18: 48,573,663-48,575,052 SMAD4
    nsv5928157copy number variation1nstd209human GRCh38 chr18: 51,048,860-51,054,778 , GRCh37.p13 chr18: 48,575,230-48,581,148 SMAD4
    nsv5711078mobile element insertion1nstd211human GRCh38 chr18: 51,079,964-51,079,964 , GRCh37.p13 chr18: 48,606,334-48,606,334 SMAD4
    nsv5673142copy number variation1nstd102humanPathogenic GRCh37 chr18: 48,593,383-48,604,842 , GRCh38.p12 chr18: 51,067,013-51,078,472 SMAD4
    nsv5673061copy number variation2nstd102humanPathogenic, Likely benign GRCh37 chr18: 48,604,616-48,604,837 , GRCh38.p12 chr18: 51,078,246-51,078,467 SMAD4
    nsv5673060copy number variation1nstd102humanLikely benign GRCh37 chr18: 48,573,407-48,573,675 , GRCh38.p12 chr18: 51,047,037-51,047,305 SMAD4
    nsv5672898copy number variation1nstd102humanLikely benign GRCh37 chr18: 48,573,411-48,604,842 , GRCh38.p12 chr18: 51,047,041-51,078,472 SMAD4
    nsv5525094copy number variation1nstd206human GRCh38 chr18: 51,058,244-51,058,339 , GRCh37.p13 chr18: 48,584,614-48,584,709 SMAD4
    nsv5519378copy number variation1nstd206human GRCh38 chr18: 51,054,995-51,058,124 , GRCh37.p13 chr18: 48,581,365-48,584,494 SMAD4
    nsv5516882copy number variation1nstd206human GRCh38 chr18: 51,076,778-51,078,255 , GRCh37.p13 chr18: 48,603,148-48,604,625 SMAD4
    nsv5514237copy number variation1nstd206human GRCh38 chr18: 51,047,297-51,048,683 , GRCh37.p13 chr18: 48,573,667-48,575,053 SMAD4
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