"GeneDx"[submitter] AND "ETV4"[gene] - ClinVar

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Search results

Items: 23

	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
Select item 777184	NM_001079675.5(ETV4):c.155-8C>T	ETV4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258836	NM_001079675.5(ETV4):c.155-117T>C	ETV4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295160	NM_001079675.5(ETV4):c.154+40AC[24]	ETV4	Microsatellite (intron variant)	not provided	GBenign
Select item 1286639	NM_001079675.5(ETV4):c.154+40AC[22]	ETV4	Microsatellite (intron variant)	not provided	GBenign
Select item 1221112	NM_001079675.5(ETV4):c.154+40AC[21]	ETV4	Microsatellite (intron variant)	not provided	GBenign
Select item 1220792	NM_001079675.5(ETV4):c.154+40AC[23]	ETV4	Microsatellite (intron variant)	not provided	GBenign
Select item 1239916	NM_001079675.5(ETV4):c.154+40AC[19]	ETV4	Microsatellite (intron variant)	not provided	GBenign
Select item 1295936	NM_001079675.5(ETV4):c.61-5C>A	ETV4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256771	NM_001079675.5(ETV4):c.-51-176C>T	ETV4	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1281545	NM_001079675.5(ETV4):c.-52+205AC[24]	ETV4	Microsatellite (intron variant)	not provided	GBenign
Select item 1225722	NM_001079675.5(ETV4):c.-52+205AC[25]	ETV4	Microsatellite (intron variant)	not provided	GBenign
Select item 1254814	NM_001079675.5(ETV4):c.-52+205AC[21]	ETV4	Microsatellite (intron variant)	not provided	GBenign
Select item 1235913	NM_001079675.5(ETV4):c.-52+205AC[22]	ETV4	Microsatellite (intron variant)	not provided	GBenign

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Items: 23