DKK2[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58033	GRCh38/hg38 4q22.3-28.3(chr4:96092893-136410207)x3	LOC129993082, LOC129993083 +661 more	Copy number gain	See cases	GPathogenic
Select item 58034	GRCh38/hg38 4q24-25(chr4:105778347-110206873)x3	AIMP1, CASP6 +106 more	Copy number gain	See cases	GPathogenic
Select item 2359347	NM_014421.3(DKK2):c.739T>A (p.Tyr247Asn)	DKK2 (Y247N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398988	NM_014421.3(DKK2):c.694G>A (p.Asp232Asn)	DKK2 (D232N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377541	NM_014421.3(DKK2):c.652C>T (p.Arg218Cys)	DKK2 (R218C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622616	NM_014421.3(DKK2):c.566G>C (p.Cys189Ser)	DKK2 (C189S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082641	NM_014421.3(DKK2):c.514A>T (p.Met172Leu)	DKK2 (M172L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272188	NM_014421.3(DKK2):c.513G>C (p.Lys171Asn)	DKK2 (K171N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082640	NM_014421.3(DKK2):c.473A>G (p.His158Arg)	DKK2 (H158R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359890	NM_014421.3(DKK2):c.311G>A (p.Arg104Gln)	DKK2 (R104Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328425	NM_014421.3(DKK2):c.301A>G (p.Met101Val)	DKK2 (M101V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218549	NM_014421.3(DKK2):c.292T>C (p.Ser98Pro)	DKK2 (S98P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317746	NM_014421.3(DKK2):c.223G>A (p.Ala75Thr)	DKK2 (A75T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462634	NM_014421.3(DKK2):c.20G>A (p.Ser7Asn)	DKK2 (S7N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558125	NM_014421.3(DKK2):c.7G>A (p.Ala3Thr)	DKK2 (A3T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2655009	NC_000004.12:g.107308018_107308019dup	DKK2	Duplication	not provided	GLikely benign
Select item 2655010	NC_000004.12:g.107308020G>A	DKK2	Single nucleotide variant	not provided	GLikely benign
Select item 2655011	NC_000004.12:g.107308037TA[2]	DKK2	Microsatellite	not provided	GLikely benign
Select item 2498958	NC_000004.12:g.107308052G>A	DKK2	Single nucleotide variant	not provided	GLikely benign
Select item 3062772	GRCh37/hg19 4q23-25(chr4:100172302-107880077)x1	ADH1A, ADH1B +34 more	Copy number loss	not specified	GPathogenic
Select item 3062767	GRCh37/hg19 4q24-35.2(chr4:101203509-190957473)x3	AADAT, ABCE1 +286 more	Copy number gain	not specified	GPathogenic
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	HPGDS, SCRG1 +537 more	Copy number gain	not provided	GPathogenic
Select item 1527114	GRCh37/hg19 4q24-31.21(chr4:104715235-145252595)	ABHD18, ADAD1 +123 more	Copy number gain	not specified	GPathogenic
Select item 1340302	GRCh37/hg19 4q22.3-25(chr4:95490755-109977216)x3	ADH1A, ADH1B +55 more	Copy number gain	not provided	GLikely pathogenic
Select item 1340288	GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3	AASDH, ABCG2 +359 more	Copy number gain	not provided	GPathogenic
Select item 814595	GRCh37/hg19 4q24-25(chr4:107693250-108066385)x3	DKK2	Copy number gain	not provided	GUncertain significance
Select item 562953	GRCh37/hg19 4q24-25(chr4:106582279-108557118)x1	NPNT, DKK2 +7 more	Copy number loss	not provided	GUncertain significance
Select item 443483	GRCh37/hg19 4q22.1-35.2(chr4:93071152-190957473)x3	AADAT, ABCE1 +314 more	Copy number gain	See cases	GPathogenic
Select item 442433	GRCh37/hg19 4q25(chr4:107918734-108514014)x4	DKK2	Copy number gain	See cases	GUncertain significance
Select item 441728	GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)	AADAT, AASDH +745 more	Copy number gain	See cases	GPathogenic
Select item 441727	GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3	MRPL1, MSANTD1 +745 more	Copy number gain	See cases	GPathogenic
Select item 394609	GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3	H2AZ1, HADH +744 more	Copy number gain	See cases	GPathogenic

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Items: 32