| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Microcephaly 6, primary, autosomal recessive +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Microcephaly 6, primary, autosomal recessive +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Microcephaly 6, primary, autosomal recessive +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | CENPJ-related condition +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Microcephaly 6, primary, autosomal recessive +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Microcephaly 6, primary, autosomal recessive +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | CENPJ-related condition +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (intron variant) | Primary Microcephaly, Recessive +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Seckel syndrome 4 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Microcephaly 6, primary, autosomal recessive +2 more | |
| | | Single nucleotide variant (intron variant) | Seckel syndrome 4 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Microcephaly 6, primary, autosomal recessive +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | CENPJ-related condition +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | CENPJ-related condition +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Microcephaly 6, primary, autosomal recessive +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | CENPJ-related condition +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | CENPJ-related condition +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Microcephaly 6, primary, autosomal recessive +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | CENPJ-related condition +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | CENPJ-related condition +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Microcephaly 6, primary, autosomal recessive +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (intron variant) | Primary Microcephaly, Recessive +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Microcephaly 6, primary, autosomal recessive +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | CENPJ-related condition +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Microcephaly 6, primary, autosomal recessive +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Microcephaly 6, primary, autosomal recessive +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Seckel syndrome 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | |