CBX7[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144164	GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3	IL17RA, LINC01640 +2088 more	Copy number gain	See cases	GPathogenic
Select item 145336	GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3	LOC130067403, LOC130067404 +2088 more	Copy number gain	See cases	GPathogenic
Select item 57942	GRCh38/hg38 22q12.3-13.33(chr22:37061769-50738932)x3	LOC130067651, LOC130067652 +1004 more	Copy number gain	See cases	GPathogenic
Select item 57943	GRCh38/hg38 22q13.1-13.2(chr22:37721797-40860953)x3	LOC130067459, LOC130067460 +273 more	Copy number gain	See cases	GPathogenic
Select item 2545781	NM_175709.5(CBX7):c.703C>T (p.Arg235Cys)	CBX7 (R142C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407193	NM_175709.5(CBX7):c.688A>G (p.Ile230Val)	CBX7 (I137V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2471797	NM_175709.5(CBX7):c.641C>T (p.Ala214Val)	CBX7 (A213V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467562	NM_175709.5(CBX7):c.616G>A (p.Glu206Lys)	CBX7 (E113K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484812	NM_175709.5(CBX7):c.611T>C (p.Leu204Pro)	CBX7 (L111P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544688	NM_175709.5(CBX7):c.609C>A (p.Asp203Glu)	CBX7 (D110E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3263687	NM_175709.5(CBX7):c.605C>T (p.Ala202Val)	CBX7 (A109V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3263686	NM_175709.5(CBX7):c.595G>A (p.Glu199Lys)	CBX7 (E106K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253210	NM_175709.5(CBX7):c.583C>G (p.Pro195Ala)	CBX7 (P195A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3263685	NM_175709.5(CBX7):c.562G>A (p.Glu188Lys)	CBX7 (E188K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3138079	NM_175709.5(CBX7):c.544G>A (p.Val182Ile)	CBX7 (V89I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357138	NM_175709.5(CBX7):c.475C>T (p.Arg159Cys)	CBX7 (R159C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3138078	NM_175709.5(CBX7):c.355A>G (p.Lys119Glu)	CBX7 (K119E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 161834	NM_175709.5(CBX7):c.227C>G (p.Pro76Arg)	CBX7 (P76R)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 2322018	NM_175709.5(CBX7):c.208A>G (p.Arg70Gly)	CBX7 (R70G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3247951	NC_000022.10:g.(?_39306081)_(41904073_?)dup	ACO2, ADSL +42 more	Duplication	Rubinstein-Taybi syndrome due to EP300 haploinsufficiency	GUncertain significance
Select item 3062450	GRCh37/hg19 22q13.1-13.31(chr22:39044105-45794212)x3	A4GALT, ACO2 +106 more	Copy number gain	not specified	GPathogenic
Select item 2422150	NC_000022.10:g.(?_35776672)_(42486826_?)dup	ACO2, ADSL +132 more	Duplication	Adenylosuccinate lyase deficiency	GUncertain significance
Select item 983188	GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3	A4GALT, ACO2 +438 more	Copy number gain	See cases	GPathogenic
Select item 816216	GRCh37/hg19 22q12.2-13.33(chr22:30654764-51197838)x3	CERK, CHADL +271 more	Copy number gain	not provided	GPathogenic
Select item 685636	GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3	TUBA8, TUBGCP6 +435 more	Copy number gain	not provided	GPathogenic
Select item 560132	Single allele	CBX7, PDGFB +4 more	Duplication	not provided	GUncertain significance
Select item 441654	GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)	ANKRD54, AP1B1 +435 more	Copy number gain	See cases	GPathogenic
Select item 441653	GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3	NEFH, NF2 +435 more	Copy number gain	See cases	GPathogenic
Select item 395140	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3	ZNF280A, ZNF280B +438 more	Copy number gain	See cases	GPathogenic
Select item 394709	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3	SMARCB1, SMC1B +438 more	Copy number gain	See cases	GPathogenic
Select item 253617	GRCh37/hg19 22q12.3-13.33(chr22:35728929-51220961)x3	A4GALT, ACO2 +223 more	Copy number gain	See cases	GPathogenic
Select item 253509	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3	A4GALT, ACO2 +438 more	Copy number gain	See cases	GPathogenic

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Items: 32