| | | Copy number loss | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Deletion | not provided | |
| | FAF2, LOC126807616 (L118V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995352, LOC129995353 +65 more | Copy number loss | Sotos syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAF2, LOC126807616 (R119C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Duplication | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAF2, LOC126807616 (S138P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAF2, LOC126807616 (T158A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAF2, LOC126807616 (E144D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Copy number gain | See cases | |
| | | Duplication | 5q35 microduplication syndrome | |
| | | Copy number gain | Hunter-McAlpine craniosynostosis | |
| | | Copy number gain | not provided | |
| | | Copy number gain | 5q35 microduplication syndrome | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | Sotos syndrome | |
| | | Deletion | Marfanoid habitus and intellectual disability | |
| | | Copy number gain | not provided | |
| | | Duplication | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | 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 | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129995362, LOC129995363 +142 more | Copy number loss | See cases | |
| | LOC129995388, LOC129995389 +145 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129995377, LOC129995378 +676 more | Copy number gain | See cases | |
| | LOC129995188, LOC129995189 +863 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129995374, LOC129995375 +136 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | FAM153A, FAM153B +176 more | Copy number gain | See cases | |
| | ADAM19, ADAMTS2 +1166 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |