Related gene-specific medical variations for Gene (Select 3050) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 869336	NC_000016.10:g.150002_180002del	HBA1, HBA2 +1 more	Deletion	alpha Thalassemia	GPathogenic
Select item 869335	NC_000016.10:g.147937_179144del	HBA1, HBA2 +1 more	Deletion	alpha Thalassemia	GPathogenic
Select item 869334	NC_000016.10:g.147601_179801del	HBA1, HBA2 +1 more	Deletion	alpha Thalassemia	GPathogenic
Select item 394388	GRCh37/hg19 16p13.3(chr16:202249-204466)x1	HBZ	Copy number loss	See cases	GBenign
Select item 394386	GRCh37/hg19 16p13.3(chr16:202249-204466)x3	HBZ	Copy number gain	See cases	GBenign

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