| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Copy number loss | See cases | |
| | LOC130055392, LOC130055393 +780 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | 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 | |
| | LOC130055370, LOC130055371 +840 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC124958012, ZNF219 (L120F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC124958012, ZNF219 (A73T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC124958012, ZNF219 (G63R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC124958012, ZNF219 (G38R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene