| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC123453201, LOC123453202 +1450 more | Copy number gain | See cases | |
| | LOC132088897, LOC132088898 +1201 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | DYNLT2B, LINC00885 +41 more | Copy number gain | See cases | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | DYNLT2B, LOC129938284 +1 more | Single nucleotide variant (intron variant) | not provided | |
| | DYNLT2B, LOC129938284 +1 more | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Copy number loss | See cases | |
Click to view in NCBI Gene