"GeneDx"[submitter] AND "DHX8"[gene] - ClinVar

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Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58696	GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3	LOC130060786, LOC130060787 +633 more	Copy number gain	See cases	GPathogenic
Select item 1243936	NM_001079675.5(ETV4):c.1231-137A>G	DHX8, ETV4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266831	NM_001079675.5(ETV4):c.1129-107C>T	DHX8, ETV4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260653	NM_001079675.5(ETV4):c.812-429CG[3]	ETV4, DHX8	Microsatellite (intron variant)	not provided	GBenign
Select item 1257943	NM_001079675.5(ETV4):c.812-428G>A	DHX8, ETV4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295940	NM_001079675.5(ETV4):c.812-454AC[9]	DHX8, ETV4	Microsatellite (intron variant)	not provided	GBenign
Select item 1241567	NM_001079675.5(ETV4):c.812-454A>T	ETV4, DHX8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249580	NM_001079675.5(ETV4):c.546-91G>A	DHX8, ETV4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241207	NM_001079675.5(ETV4):c.256+285GTTT[5]	DHX8, ETV4	Microsatellite (intron variant)	not provided	GBenign
Select item 1274156	NM_001079675.5(ETV4):c.256+103C>A	DHX8, ETV4	Single nucleotide variant (intron variant)	not provided	GBenign