"GeneDx"[submitter] AND "FHIT"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57731	GRCh38/hg38 3p14.2(chr3:59743673-60984329)x3	FHIT, LOC107325936 +9 more	Copy number gain	See cases	GUncertain significance
Select item 144862	GRCh38/hg38 3p14.2(chr3:60102627-60254729)x1	FHIT	Copy number loss	See cases	GBenign
Select item 60084	GRCh38/hg38 3p14.2(chr3:60460013-60532126)x1	FHIT, LOC107325936	Copy number loss	See cases	GUncertain significance
Select item 60085	GRCh38/hg38 3p14.2(chr3:61173973-61402744)x1	FHIT, LOC112935954 +9 more	Copy number loss	See cases	GUncertain significance
Select item 253794	GRCh37/hg19 3p14.3-14.2(chr3:58494677-60076736)x3	FHIT, NPCDR1 +4 more	Copy number gain	See cases	GUncertain significance

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