ClinVar (all) for Orgtrack (Select 509430) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063596	NC_000023.10:g.154182167_154227754inv	F8	Inversion	Hereditary factor VIII deficiency disease	GPathogenic
Select item 3062367	NC_000023.11:g.154161393_154377600dup	FLNA, LOC107988032 +14 more	Duplication	Hereditary factor VIII deficiency disease	GPathogenic