| | LOC130057816, LOC130057817 +1763 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC111822949, LOC112272574 +664 more | Copy number gain | See cases | |
| | LOC130057971, LOC130057972 +630 more | Copy number gain | See cases | |
| | LOC130057938, LOC130057939 +611 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130057962, LOC130057963 +517 more | Copy number gain | See cases | |
| | LOC130058025, LOC130058026 +500 more | Copy number gain | See cases | |
| | ADAMTS17, ALDH1A3 +422 more | Copy number gain | See cases | |
| | ADAMTS17, ALDH1A3 +228 more | Copy number gain | See cases | |
| | ADAMTS17, ALDH1A3 +224 more | Copy number loss | See cases | |
| | ADAMTS17, ALDH1A3 +205 more | Copy number loss | See cases | |
| | ADAMTS17, ALDH1A3 +218 more | Copy number gain | See cases | |
| | LOC130058035, LOC130058036 +202 more | Copy number loss | See cases | |
| | LOC126862250, LOC126862251 +203 more | Copy number loss | See cases | |
| | ADAMTS17, ALDH1A3 +201 more | Copy number loss | See cases | |
| | ADAMTS17, ALDH1A3 +195 more | Copy number loss | See cases | |
| | ADAMTS17, ALDH1A3 +184 more | Copy number loss | See cases | |
| | ADAMTS17, ALDH1A3 +185 more | Copy number loss | See cases | |
| | ADAMTS17, ALDH1A3 +184 more | Copy number gain | See cases | |
| | ADAMTS17, ALDH1A3 +179 more | Copy number loss | See cases | |
| | ADAMTS17, ALDH1A3 +174 more | Copy number loss | See cases | |
| | ADAMTS17, ARRDC4 +111 more | Copy number gain | See cases | |
| | ADAMTS17, ALDH1A3 +171 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | ADAMTS17, ALDH1A3 +165 more | Copy number gain | See cases | |
| | ADAMTS17, ALDH1A3 +159 more | Copy number loss | See cases | |
| | LOC130058072, LOC130058073 +148 more | Copy number loss | See cases | |
| | IGF1R, LOC126862245 +24 more | Copy number gain | See cases | |
| | IGF1R, LOC126862245 +18 more | Copy number loss | See cases | |
| | IGF1R, LOC130058004 +17 more | Copy number loss | See cases | |
| | IGF1R, LOC130058004 +17 more | Copy number loss | See cases | |
| | LINC02244, LOC105371017 +35 more | Copy number gain | See cases | |
| | LINC02244, LOC105371017 +25 more | Copy number gain | See cases | |
| | LINC02244, LOC105371017 +30 more | Copy number gain | See cases | |
| | LOC126862246, LOC129390743 +11 more | Copy number gain | See cases | |
| | LOC130058014, SYNM +1 more (E14D) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more | Single nucleotide variant (synonymous variant) | SYNM-related condition | |
| | LOC130058014, SYNM +1 more | Single nucleotide variant (synonymous variant) | SYNM-related condition | |
| | LOC130058014, SYNM +1 more | Single nucleotide variant (synonymous variant) | SYNM-related condition | |
| | LOC130058014, SYNM +1 more (G45C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (R46W) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more | Single nucleotide variant (synonymous variant) | SYNM-related condition | |
| | LOC130058014, SYNM +1 more (G56R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (E73Q) | Single nucleotide variant (missense variant) | SYNM-related condition | |
| | LOC130058014, SYNM +1 more (G83D) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more | Single nucleotide variant (synonymous variant) | SYNM-related condition | |
| | LOC130058014, SYNM +1 more (E94K) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (E94D) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (D110N) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more | Single nucleotide variant (synonymous variant) | SYNM-related condition | |
| | LOC130058014, SYNM +1 more (A115V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (Q117L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (Q117H) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (Q121P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (G125R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more | Single nucleotide variant (synonymous variant) | SYNM-related condition | |
| | LOC130058014, SYNM +1 more (D145A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (A146E) | Single nucleotide variant (missense variant) | not specified | |
| | SYNM, SYNM-AS1 +1 more (H148P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (D151A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (D151E) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more | Single nucleotide variant (synonymous variant) | SYNM-related condition | |
| | LOC130058014, SYNM +1 more (R156C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC130058014, SYNM +1 more (L162V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (H165Y) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more (R167C) | Single nucleotide variant (non-coding transcript variant +1 more) | SYNM-related condition | |
| | LOC130058014, SYNM +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | SYNM-related condition | |
| | LOC130058014, SYNM +1 more (P176A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058014, SYNM +1 more | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | SYNM-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | SYNM-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | SYNM-related condition | |
| | | Single nucleotide variant (synonymous variant) | SYNM-related condition | |
| | | Duplication (frameshift variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | SYNM-related condition | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | SYNM-related condition | |
| | | Single nucleotide variant (missense variant) | SYNM-related condition | |
| | | Single nucleotide variant (missense variant) | SYNM-related condition | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | SYNM-related condition | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | SYNM-related condition | |