| | LOC112533659, LOC112533660 +2032 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC121852934, CRHR1 +9 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC121852934, CRHR1 +10 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC121852934, CRHR1 +9 more | 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 | |
| | LOC121852934, CRHR1 +9 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | CRHR1, LINC02210-CRHR1 +6 more | Copy number gain | See cases | |
| | CRHR1, LINC02210-CRHR1 +6 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | MAPT-Related Spectrum Disorders | |
| | | Deletion (5 prime UTR variant +1 more) | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant (intron variant) | Frontotemporal dementia | |
| | | 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 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | MAPT-Related Spectrum Disorders +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (missense variant +1 more) | Supranuclear palsy, progressive, 1 +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Supranuclear palsy, progressive, 1 | |
| | | Single nucleotide variant (missense variant +1 more) | MAPT-Related Spectrum Disorders +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (missense variant +1 more) | Parkinson disease, late-onset +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Malignant tumor of prostate | |
| | | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia +1 more | GConflicting classifications of pathogenicity |
| | | Indel (missense variant +1 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Malignant tumor of prostate | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frontotemporal dementia +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Frontotemporal dementia +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (intron variant) | Frontotemporal dementia | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Insertion (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Frontotemporal dementia | |
| | | Single nucleotide variant (missense variant +2 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (missense variant +2 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (synonymous variant +2 more) | MAPT-Related Spectrum Disorders | |
| | | Single nucleotide variant (missense variant +2 more) | Frontotemporal dementia +2 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (synonymous variant +2 more) | Frontotemporal dementia | |
| | | Single nucleotide variant (missense variant +2 more) | MAPT-related disorder | |
| | | Single nucleotide variant (synonymous variant +2 more) | Frontotemporal dementia | |
| | | Deletion (intron variant) | Frontotemporal dementia | |