| | A3GALT2, ACOT11 +1226 more | Inversion | Bilateral polymicrogyria | |
| | | Single nucleotide variant (3 prime UTR variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Deletion (3 prime UTR variant) | Primary Microcephaly, Recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | Microcephaly 7, primary, autosomal recessive +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Microcephaly 7, primary, autosomal recessive +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (nonsense) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (nonsense) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Duplication (frameshift variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Microsatellite (nonsense) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Microsatellite (frameshift variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive +2 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | Microcephaly 7, primary, autosomal recessive +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive +1 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (synonymous variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (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 (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | Microcephaly 7, primary, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |