| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861884, NDRG2 (N219H +3 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861884, NDRG2 (I210T +3 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861884, NDRG2 (H184R +3 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861884, NDRG2 (H223R +3 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | See cases | |
| | LOC126861920, LOC126861921 +3280 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 | |
| | LOC130055392, LOC130055393 +780 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC130055370, LOC130055371 +840 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
Click to view in NCBI Gene