Related gene-specific medical variations for Gene (Select 7516) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3245890	NC_000007.14:g.(?_152648642)_(152649373_?)dup	XRCC2	Duplication	not provided	GUncertain significance
Select item 3245889	NC_000007.14:g.(?_152648642)_(152676080_?)dup	XRCC2	Duplication	not provided	GUncertain significance
Select item 3245887	NC_000007.13:g.(?_152345727)_(152357877_?)del	XRCC2	Deletion	not provided	GUncertain significance
Select item 3245886	NC_000007.13:g.(?_152357776)_(152357877_?)del	XRCC2	Deletion	not provided	GUncertain significance
Select item 3245885	NC_000007.13:g.(?_152373106)_(152373164_?)del	XRCC2	Deletion	not provided	GUncertain significance
Select item 2682134	NM_005431.2(XRCC2):c.290A>G (p.Glu97Gly)	XRCC2 (E97G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1763162	NM_005431.1:c.838_839insALU	XRCC2	Insertion	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1319870	NM_005431.2(XRCC2):c.213A>C (p.Glu71Asp)	XRCC2 (E71D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 685492	GRCh37/hg19 7q36.1(chr7:152316248-152441752)x3	XRCC2	Copy number gain	not provided	GUncertain significance

ClinVar