| | LOC123477714, LOC123477715 +1267 more | Copy number gain | Neurodevelopmental disorder | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129991977, LOC129991978 +283 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129992145, LOC129992146 +1209 more | Copy number gain | See cases | |
| | AFAP1, AFAP1-AS1 +633 more | 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 gain | See cases | |
| | LOC129991962, LOC129991963 +137 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | CTBP1-AS, CTBP1-DT +278 more | Copy number loss | See cases | |
| | LOC129992028, LOC129992029 +691 more | Copy number loss | See cases | |
| | LOC129992002, LOC129992003 +597 more | Copy number loss | See cases | |
| | LOC101928279, LOC101928306 +346 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129992008, LOC129992009 +175 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC126806993, LOC126806994 +702 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129992237, LOC129992238 +861 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129991980, LOC129991981 +319 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC123466217, LOC123466218 +277 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129992157, LOC129992158 +832 more | 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 | |
| | LOC129992049, LOC129992050 +537 more | Copy number loss | See cases | |
| | LOC129992097, LOC129992098 +256 more | Copy number loss | 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 | See cases | |
| | | Copy number loss | See cases | |
| | LOC129992176, LOC129992177 +439 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129992561, LOC129992562 +1409 more | Copy number gain | Neurodevelopmental disorder | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129991981, LOC129991982 +206 more | Copy number gain | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | RNF212-related disorder | |
| | | Single nucleotide variant (intron variant) | RNF212-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | RNF212-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | RNF212-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | RNF212-related disorder | |
| | | Deletion (intron variant) | RNF212-related disorder | |
| | | Single nucleotide variant (intron variant) | RNF212-related disorder | |
| | | Single nucleotide variant (missense variant) | RNF212-related disorder | |
| | | Single nucleotide variant (missense variant) | RNF212-related disorder | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +3 more) | not specified | |
| | | Single nucleotide variant (missense variant +3 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (intron variant) | Recombination rate quantitative trait locus 1 | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | Breast ductal adenocarcinoma | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Deletion (frameshift variant +1 more) | Non-obstructive azoospermia | |
| | | Single nucleotide variant (nonsense +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 | |
| | | Single nucleotide variant (intron variant) | Recombination rate quantitative trait locus 1 | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |