| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126862863, LOC126862864 +536 more | Copy number gain | See cases | |
| | PPAN, PPAN-P2RY11 +184 more | Copy number loss | See cases | |
| | LOC130063493, LOC130063494 +116 more | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
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