DUSP3[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 148363	GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3	LOC112533659, LOC112533660 +2032 more	Copy number gain	See cases	GPathogenic
Select item 57282	GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3	AARSD1, AATF +1753 more	Copy number gain	See cases	GPathogenic
Select item 58696	GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3	AARSD1, ACBD4 +633 more	Copy number gain	See cases	GPathogenic
Select item 155568	GRCh38/hg38 17q21.31(chr17:43050945-43897883)x3	ARL4D, BRCA1 +52 more	Copy number gain	See cases	GUncertain significance
Select item 148621	GRCh38/hg38 17q21.31(chr17:43080123-43897875)x3	ARL4D, BRCA1 +52 more	Copy number gain	See cases	GUncertain significance
Select item 150167	GRCh38/hg38 17q21.31(chr17:43088882-43865172)x3	ARL4D, BRCA1 +50 more	Copy number gain	See cases	GUncertain significance
Select item 154024	GRCh38/hg38 17q21.31(chr17:43322528-43849385)x3	ARL4D, CD300LG +33 more	Copy number gain	See cases	GLikely benign
Select item 148000	GRCh38/hg38 17q21.31(chr17:43387123-43865083)x3	ARL4D, CD300LG +26 more	Copy number gain	See cases	GUncertain significance
Select item 59586	GRCh38/hg38 17q21.31(chr17:43570878-44762377)x1	ADAM11, ASB16 +104 more	Copy number loss	See cases	GPathogenic
Select item 2499654	GRCh38/hg38 17q21.31(chr17:43603558-44033313)	CD300LG, CFAP97D1 +29 more	Copy number gain	Anomalous pulmonary venous return	GUncertain significance
Select item 3086327	NM_004090.4(DUSP3):c.364G>A (p.Val122Ile)	DUSP3 (V122I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602619	NM_004090.4(DUSP3):c.356G>A (p.Arg119Gln)	DUSP3 (R119Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086326	NM_004090.4(DUSP3):c.325A>G (p.Ile109Val)	DUSP3 (I109V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409247	NM_004090.4(DUSP3):c.244G>A (p.Gly82Ser)	DUSP3 (G82S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380356	NM_004090.4(DUSP3):c.221A>G (p.Asn74Ser)	DUSP3 (N74S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2647815	NM_004090.4(DUSP3):c.183C>T (p.Asn61=)	DUSP3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3086329	NM_004090.4(DUSP3):c.55G>A (p.Gly19Ser)	DUSP3, LOC112533640 (G19S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1526577	GRCh37/hg19 17q21.31(chr17:41202796-41974964)	ARL4D, BRCA1 +12 more	Copy number gain	not specified	GUncertain significance
Select item 815937	GRCh37/hg19 17q21.31(chr17:41399892-42125780)x3	ARL4D, CD300LG +13 more	Copy number gain	not provided	GUncertain significance
Select item 688227	GRCh37/hg19 17q21.31(chr17:41800157-41903109)x1	CFAP97D1, DUSP3 +2 more	Copy number loss	not provided	GUncertain significance
Select item 564447	GRCh37/hg19 17q21.31(chr17:41540257-42044249)x1	CD300LG, CFAP97D1 +9 more	Copy number loss	not provided	GUncertain significance
Select item 441816	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	EFTUD2, EIF1 +1143 more	Copy number gain	See cases	GPathogenic
Select item 441815	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	KRT15, KRT16 +1143 more	Copy number gain	See cases	GPathogenic

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Items: 23