"Counsyl"[submitter] AND "HBA1"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 487442	NC_000016.10:g.(?_151209)_(182142_?)del	LOC130058091, HBA-LCR +8 more	Deletion	alpha Thalassemia	GPathogenic
Select item 487448	NC_000016.10:g.(?_169780)_(182142_?)del	HBA2, HBQ1 +5 more	Deletion	alpha Thalassemia	GPathogenic
Select item 433555	Single allele	HBA1, HBA2 +2 more	Deletion	alpha Thalassemia	GPathogenic

Format

Sort by

Choose Destination