| | LOC129932995, LOC129932996 +653 more | Copy number gain | See cases | |
| | LOC126806176, LOC126806177 +1047 more | Copy number gain | See cases | |
| | LOC129933180, LOC129933181 +498 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126806115, LOC126806116 +237 more | Copy number gain | See cases | |
| | LOC129933242, LOC129933243 +1631 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126806154, LOC126806155 +546 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129934199, LOC129934200 +2457 more | Copy number gain | See cases | |
| | | Deletion | Neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | 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) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | not specified +2 more | |
| | | Deletion (3 prime UTR variant) | not specified +2 more | |
| | ADAM17, IAH1 (V518fs +2 more) | Deletion (frameshift variant) | Inborn genetic diseases | |
| | | Duplication (inframe_insertion) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (T523fs +2 more) | Deletion (frameshift variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (D519H +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (R517fs +2 more) | Duplication (frameshift variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (N516S +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (R593H +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (F809L +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (A586S +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | IAH1, ADAM17 (A586fs +2 more) | Duplication (frameshift variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (E505G +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | IAH1, ADAM17 (D498fs +2 more) | Deletion (frameshift variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (D577Y +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (L496V +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 +1 more | |
| | ADAM17, IAH1 (S550fs +2 more) | Deletion (frameshift variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (S770P +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (Q464R +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (H457Q +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (A452P +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | IAH1, ADAM17 (A530T +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (S448L +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 +1 more | |
| | ADAM17, IAH1 (S527fs +2 more) | Duplication (frameshift variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (P444A +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (A443T +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (Q520P +2 more) | Indel (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (R518H +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (A433V +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (P432S +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (P511A +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (F431L +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (V425fs +2 more) | Deletion (frameshift variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (R426H +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (R505fs +2 more) | Insertion (frameshift variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | ADAM17, IAH1 (S503L +2 more) | Single nucleotide variant (missense variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (intron variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (intron variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (intron variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Microsatellite (intron variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Microsatellite (intron variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (intron variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (intron variant) | Inflammatory skin and bowel disease, neonatal, 1 | |
| | | Single nucleotide variant (intron variant) | Inflammatory skin and bowel disease, neonatal, 1 | |