| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861125, TIMM10B (Q6E) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861125, TIMM10B (M64L) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861125, TIMM10B (Q4P) | Single nucleotide variant (missense variant) | not specified | |
| | C11orf42, MRGPRG +210 more | Copy number gain | Russell-Silver syndrome | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Duplication | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | not provided | |
| | | Duplication | not provided | |
| | | Copy number gain | Silver-Russell syndrome 1 | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | Silver-Russell syndrome 1 | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | 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 | |
| | LOC130005128, LOC130005129 +723 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
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