| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129995709, LOC129995710 +642 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LINC01600, LINC01622 +308 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LINC01622, LINC02521 +558 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129995671, LOC129995672 +509 more | Copy number gain | See cases | |
| | LOC129995581, LOC129995582 +436 more | Copy number gain | See cases | |
| | KU-MEL-3, LINC01011 +302 more | Copy number loss | See cases | |
| | LOC129995556, LOC129995570 +306 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129389424, LOC129389425 +311 more | Copy number loss | See cases | |
| | BLOC1S5, BLOC1S5-TXNDC5 +432 more | Copy number loss | See cases | |
| | LOC126859578, LOC126859579 +536 more | Copy number gain | See cases | |
| | | Inversion | Anophthalmia-microphthalmia syndrome | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC643327, PRPF4B +31 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129995677, LOC129995678 +331 more | Copy number loss | See cases | |
| | | Single nucleotide variant (non-coding transcript variant) | not specified | |
| | | Single nucleotide variant (non-coding transcript variant) | not specified | |
| | C6orf201, ECI2 (V384M +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (P342Q +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (F326S +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (P322S +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | C6orf201, ECI2 (A278E +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (M299V +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (K295T +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (K289R +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (A232V +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (V260M +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (I219T +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (F201S +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | C6orf201, ECI2 +1 more (A191T +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 +1 more (P209T +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 +1 more (T206I +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 +1 more (D194N +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (I134V +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (I150V +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (T107A +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (Y81C +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C6orf201, ECI2 (Y81H +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Copy number loss | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Duplication | not provided | |
| | | Copy number gain | See cases | |
| | | 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 gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |