| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130064925, LOC130064926 +1081 more | Copy number gain | See cases | |
| | LOC130064903, LOC130064904 +1093 more | Copy number gain | See cases | |
| | LOC130065082, LOC130065083 +806 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130065034, LOC130065035 +761 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Deletion | not provided | |
| | LOC112553116, NLRP11 (T345M +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC112553116, NLRP11 (L341F +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC112553116, NLRP11 (I232M +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC112553116, NLRP11 (A319T +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC112553116, NLRP11 (R281C +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC112553116, NLRP11 (R182G +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
Click to view in NCBI Gene