Related gene-specific medical variations for Gene (Select 92521) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 873216	NM_001243439.2(SPECC1):c.3118-1937T>G	SPECC1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 442943	GRCh37/hg19 17p11.2(chr17:19947920-20194183)x1	SPECC1	Copy number loss	See cases	GUncertain significance
Select item 395093	GRCh37/hg19 17p11.2(chr17:20096001-20232061)x3	SPECC1	Copy number gain	See cases	GUncertain significance
Select item 395049	GRCh37/hg19 17p11.2(chr17:19947875-19986611)x3	SPECC1	Copy number gain	See cases	GBenign

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