"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "HBA2"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 648517	NC_000016.10:g.(?_172913)_(177411_?)del	HBA1, HBA2 +2 more	Deletion	not provided	GPathogenic
Select item 639866	NC_000016.10:g.(?_172913)_(173600_?)del	HBA2, LOC106804612	Deletion	not provided	GPathogenic
Select item 725759	NM_000517.6(HBA2):c.414C>T (p.Thr138=)	HBA2, LOC106804612	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 15653	NM_000517.4(HBA2):c.427T>G (p.Ter143Glu)	HBA2, LOC106804612	Single nucleotide variant (stop lost)	not provided	GPathogenic/Likely pathogenic
Select item 15626	NM_000517.4(HBA2):c.427T>A (p.Ter143Lys)	HBA2, LOC106804612	Single nucleotide variant (stop lost)	alpha Thalassemia +2 more	GPathogenic
Select item 15624	NM_000517.4(HBA2):c.427T>C (p.Ter143Gln)	HBA1, HBA2 +1 more	Single nucleotide variant (stop lost)	Erythrocytosis, familial, 7 +4 more	GPathogenic
Select item 2423327	NC_000016.9:g.(?_222912)_(226810_?)del	HBA2, HBA1	Deletion	not provided	GPathogenic
Select item 1459499	NC_000016.9:g.(?_97132)_(163851_?)del	HBA2, MPG +4 more	Deletion	not provided	GPathogenic
Select item 1072685	NC_000016.9:g.(?_163493)_(193701_?)del	HBA2, NPRL3	Deletion	not provided	GPathogenic
Select item 1072684	NC_000016.9:g.(?_163493)_(163851_?)del	HBA2, NPRL3	Deletion	not provided	GPathogenic
Select item 831357	NC_000016.9:g.(?_97132)_(193701_?)del	HBA2, MPG +4 more	Deletion	not provided	GPathogenic