| | | Copy number gain | See cases | |
| | LOC126860768, LOC126860769 +3785 more | Copy number gain | See cases | |
| | LOC130001533, LOC130001534 +1213 more | Copy number gain | See cases | |
| | LOC124310660, LOC124310661 +3784 more | Copy number gain | See cases | |
| | LOC111413024, LOC111413033 +3785 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC116216098, LOC116216099 +3785 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | DAPK1-IT1, DCAF10 +1366 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130001787, LOC130001788 +983 more | Copy number gain | See cases | |
| | LOC130001685, LOC130001686 +898 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126860765, LOC126860766 +3785 more | Copy number gain | See cases | |
| | LOC126860590, LOC126860591 +897 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130001651, LOC130001652 +585 more | Copy number gain | See cases | |
| | LOC130001669, LOC130001670 +690 more | Copy number gain | See cases | |
| | LOC130001706, LOC130001707 +435 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130001670, LOC130001671 +360 more | Copy number gain | See cases | |
| | LOC130001763, LOC730098 +211 more | Copy number loss | See cases | |
| | LOC129662434, LOC130001682 +138 more | Duplication | Anauxetic dysplasia | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Duplication (3 prime UTR variant) | Inclusion Body Myopathy, Dominant +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Deletion (3 prime UTR variant) | Amyotrophic Lateral Sclerosis, Dominant +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +5 more | |
| | | Single nucleotide variant (missense variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (synonymous variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +2 more | |
| | | Single nucleotide variant (synonymous variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (intron variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (intron variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (intron variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (synonymous variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (missense variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +5 more | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +2 more | GConflicting classifications of pathogenicity |