| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | FAM95B1, FAM95C +1214 more | Copy number gain | See cases | |
| | LOC129390066, LOC129390067 +3785 more | Copy number gain | See cases | |
| | LOC126860762, LOC126860763 +3786 more | Copy number gain | See cases | |
| | LOC124292579, LOC124292580 +3786 more | Copy number gain | See cases | |
| | LOC130001496, LOC130001497 +1062 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | DENND4C, DIPK1B +3786 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130001660, LOC130001661 +3786 more | Copy number gain | See cases | |
| | LOC126860587, LOC126860588 +3786 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | SPATA31A5, SPATA31A6 +980 more | Copy number gain | See cases | |
| | LINC01235, LINC01239 +899 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130001820, LOC130001821 +899 more | Copy number gain | See cases | |
| | LOC130001624, LOC130001625 +894 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | SLC24A2, SLC25A51 +691 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Duplication | not provided | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not provided | |
| | | Duplication | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Duplication | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Syndromic anorectal malformation | |
| | | Copy number gain | MISSED ABORTION | |
| | | Copy number loss | Distal tetrasomy 15q | |
| | | Copy number gain | Bradycardia | |
| | | Copy number gain | Tetrasomy 9p | |
| | | Copy number gain | not specified | |
| | ANKRD18A, ANKRD18B +768 more | Copy number gain | not specified | |
| | SPATA31A5, SPATA31A6 +257 more | Copy number gain | not specified | |
| | | Copy number gain | not specified | |
| | | Duplication | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Inversion | Abnormal chromosome morphology +1 more | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Complex | Glioma | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | CNTNAP3, CNTNAP3B +204 more | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | Syndromic hydrocephalus due to diffuse villous hyperplasia of choroid plexus | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |