Related gene-specific medical variations for Gene (Select 7852) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1319371	NM_003467.3(CXCR4):c.1025_1028del (p.Thr342fs)	CXCR4 (T327fs +4 more)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 636688	NM_003467.3(CXCR4):c.786C>A (p.Asp262Glu)	CXCR4 (D262E +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 562541	GRCh37/hg19 2q21.3-22.1(chr2:136770508-136973781)x1	CXCR4	Copy number loss	not provided	GUncertain significance

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