| | LOC130003185, LOC130003186 +680 more | Copy number loss | See cases | |
| | LINC02645, LINC02648 +496 more | Copy number gain | See cases | |
| | ADARB2, ADARB2-AS1 +276 more | Copy number loss | See cases | |
| | LOC126860819, LOC126860820 +680 more | Copy number gain | See cases | |
| | LOC124403900, LOC124403901 +520 more | Copy number loss | See cases | |
| | LOC132090805, MANCR +482 more | Copy number gain | See cases | |
| | LINC00700, LINC00701 +837 more | Copy number gain | See cases | |
| | LOC132089789, LOC132089790 +421 more | Copy number gain | See cases | |
| | ADARB2, ADARB2-AS1 +298 more | Copy number gain | See cases | |
| | ADARB2, ADARB2-AS1 +352 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130003188, LOC130003189 +195 more | Duplication | Schizophrenia | |
| | LOC130003254, LOC130003255 +1221 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC130003217, LOC130003218 +482 more | Copy number loss | See cases | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | IL15RA, LOC130003225 (L20P +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | IL15RA, LOC130003225 (R42C +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | IL15RA, LOC130003225 (P38L +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number gain | Mosaic supernumerary isodicentric chromosome 10 | |
| | | Deletion | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Deletion | Hypoparathyroidism, deafness, renal disease syndrome | |
| | | Copy number gain | 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 | |