Related gene-specific medical variations for Gene (Select 55253) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 814978	GRCh37/hg19 7q11.21(chr7:66598046-66998502)x3	TYW1	Copy number gain	not provided	GUncertain significance
Select item 563312	GRCh37/hg19 7q11.21(chr7:66629226-66788040)x1	TYW1	Copy number loss	not provided	GLikely benign
Select item 394934	GRCh37/hg19 7q11.21(chr7:66582870-66760808)x3	TYW1	Copy number gain	See cases	Gconflicting data from submitters
Select item 394443	GRCh37/hg19 7q11.21(chr7:66582870-66771054)x3	TYW1	Copy number gain	See cases	GLikely benign

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