| | LOC121466733, LOC121468000 +2048 more | Copy number loss | See cases | |
| | LOC130010147, LOC130010148 +2049 more | Copy number gain | See cases | |
| | LOC130009360, LOC130009361 +2047 more | Copy number gain | See cases | |
| | LOC130009909, LOC130009910 +2044 more | Copy number gain | See cases | |
| | LINC00333, LINC00343 +2045 more | Copy number gain | See cases | |
| | LOC112163664, LOC112163665 +2040 more | Copy number gain | See cases | |
| | LOC121838573, LOC121838574 +2028 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LINC00462, LINC00463 +2021 more | Copy number gain | See cases | |
| | | 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 | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LINC00434, LINC00437 +735 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 | |
| | | Copy number loss | See cases | |
| | LOC130009641, LOC130009642 +141 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC130009906, LOC130009907 +733 more | Copy number loss | See cases | |
| | LINC00561, LINC00562 +729 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 | |
| | LOC126861752, TNFSF11 (S7L +1 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC126861752, TNFSF11 (H12R +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861752, TNFSF11 (H85L +1 more) | Single nucleotide variant (missense variant) | Autosomal recessive osteopetrosis 2 | |
| | LOC126861752, TNFSF11 (Y15C +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861752, TNFSF11 (I90V +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC126861752, TNFSF11 (D98H +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC126861752, TNFSF11 (T103I +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC126861752, TNFSF11 (T36I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861752, TNFSF11 (S42L +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861752, TNFSF11 (R117K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861752, TNFSF11 (R118I +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | TNFSF11-related disorder | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Indel (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |