| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861648, LOC126861649 +4836 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | ZNF664, ZNF664-RFLNA +786 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC130009168, LOC130009169 +408 more | Copy number gain | See cases | |
| | ADGRD1, ADGRD1-AS1 +266 more | Copy number gain | See cases | |
| | GLT1D1, LINC00507 +43 more | Copy number gain | See cases | |
| | GLT1D1, LOC100128276 +30 more | Copy number gain | See cases | |
| | GLT1D1, LOC100128276 +28 more | Copy number gain | See cases | |
| | GLT1D1, LOC126861685 (L133M +4 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | GLT1D1, LOC126861685 (V279M +4 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
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