| | ARMCX5-GPRASP2, GPRASP3 (M316I) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (K315E) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (P313L) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (N305S) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (R282C) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (A256T) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (N189K) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (E171K) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (A109V) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (K59E) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (L528M) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (T476A) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (N457I) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (I428T) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (T40P) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (K383T) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (N352S) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | ARMCX5-GPRASP2, GPRASP3 (N189H) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | ARMCX5-GPRASP2, GPRASP3 (V33G) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (I119T) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (T546R) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (R272G) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | Klinefelter syndrome | |
| | ARMCX5-GPRASP2, GPRASP3 (A311V) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (I247V) | Single nucleotide variant (missense variant) | not specified | |
| | ARMCX5-GPRASP2, GPRASP3 (T336A) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | Klinefelter syndrome | |
| | | Copy number loss | Turner syndrome | |
| | | Copy number loss | Turner syndrome | |
| | | Copy number gain | Hypotonia +2 more | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not specified | |
| | ARMCX5, ARMCX5-GPRASP2 +21 more | Copy number loss | not specified | |
| | CXorf51B, GAGE12H +821 more | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | Xq21.32q23 deletion | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | ARMCX5-GPRASP2, GPRASP3 (Y319S) | Single nucleotide variant (missense variant) | not provided | |
| | ARMCX5-GPRASP2, GPRASP3 (C318R) | Single nucleotide variant (missense variant) | not provided | |
| | | Copy number loss | Early Onset Neurological Disease Trait | |
| | | Copy number loss | Early Onset Neurological Disease Trait | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Duplication | Syndromic X-linked intellectual disability Lubs type | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Indel | Heterotaxy, visceral, 1, X-linked | |
| | LOC130068573, LOC130068624 +2631 more | Duplication | Schizophrenia +1 more | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | 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 loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | not provided | |
| | FAM133A, FAM156A +819 more | 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 gain | See cases | |
| | | Copy number gain | See cases | |
| | CT47A11, CT47A12 +818 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | GAGE12F, GAGE12G +822 more | Copy number gain | See cases | |