| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | Microcephaly 5, primary, autosomal recessive | |
| | | Indel (frameshift variant +1 more) | Microcephaly 5, primary, autosomal recessive | |
| | | Deletion (frameshift variant +1 more) | Inborn genetic diseases +2 more | |
| | | Deletion (frameshift variant +1 more) | Inborn genetic diseases +3 more | |
| | | Microsatellite (frameshift variant +1 more) | not provided +1 more | |
| | | Duplication (frameshift variant +1 more) | Microcephaly 5, primary, autosomal recessive | |
| | | Microsatellite (frameshift variant +1 more) | Microcephaly 5, primary, autosomal recessive | |
| | | Microsatellite (nonsense +1 more) | Microcephaly 5, primary, autosomal recessive | |
| | | Duplication (frameshift variant +1 more) | Microcephaly 5, primary, autosomal recessive | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Microcephaly 5, primary, autosomal recessive +1 more | |
| | | Deletion (frameshift variant) | Microcephaly 5, primary, autosomal recessive | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Microcephaly 5, primary, autosomal recessive | |
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