ClinVar for Gene (Select 284124) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155479	GRCh38/hg38 17p11.2-11.1(chr17:22181582-22762465)x1	FAM27E5, FLJ36000 +4 more	Copy number loss	See cases	Gconflicting data from submitters
Select item 153544	GRCh38/hg38 17p11.2-11.1(chr17:22140003-22762465)x3	FAM27E5, FLJ36000 +4 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 151199	GRCh38/hg38 17p11.2(chr17:22159041-22672350)x1	FAM27E5, FLJ36000 +4 more	Copy number loss	See cases	GUncertain significance
Select item 148725	GRCh38/hg38 17p11.2-11.1(chr17:22156481-22726994)x1	FAM27E5, FLJ36000 +4 more	Copy number loss	See cases	GLikely benign
Select item 148602	GRCh38/hg38 17p11.2-11.1(chr17:22159041-22726994)x1	FAM27E5, FLJ36000 +4 more	Copy number loss	See cases	Gconflicting data from submitters
Select item 145459	GRCh38/hg38 17p11.2-11.1(chr17:22209684-22706517)x1	FAM27E5, FLJ36000 +4 more	Copy number loss	See cases	GBenign/Likely benign
Select item 145458	GRCh38/hg38 17p11.2-11.1(chr17:22209684-22706517)x3	FAM27E5, FLJ36000 +4 more	Copy number gain	See cases	GBenign
Select item 59297	GRCh38/hg38 17p11.2(chr17:20879426-22533437)x3	CCDC144NL-AS1, DHRS7B +41 more	Copy number gain	See cases	GUncertain significance
Select item 58296	GRCh38/hg38 17p11.2-11.1(chr17:22156481-22706494)x1	FAM27E5, FLJ36000 +4 more	Copy number loss	See cases	GUncertain significance

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