| | AMOTL2, DNAJC13 +1343 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | Chromosome 3q13.31 deletion syndrome | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129937263, LOC129937264 +247 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant (nonsense) | Hypotrichosis 15 | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Deletion (frameshift variant +1 more) | Hypotrichosis 15 | |
| | | Single nucleotide variant (splice donor variant +1 more) | not provided | |
| | | Single nucleotide variant (nonsense +1 more) | Hypotrichosis 15 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Deletion (frameshift variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C3orf52, GCSAM (R165C +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C3orf52, GCSAM (Y150N +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C3orf52, GCSAM (T121A +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C3orf52, GCSAM (R116T +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C3orf52, GCSAM (Y82D +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C3orf52, GCSAM (P56T +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C3orf52, GCSAM (K52N +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C3orf52, GCSAM (A40T +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C3orf52, GCSAM (M26I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number loss | Chromosome 3q13.31 deletion syndrome | |
| | | Copy number loss | not provided | |
| | | Copy number loss | Chromosome 3q13.31 deletion syndrome | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |