ClinVar for Gene (Select 101927728) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151500	GRCh38/hg38 17q22-23.1(chr17:57418806-59735464)x1	C17orf47, CCDC182 +168 more	Copy number loss	See cases	GPathogenic
Select item 150741	GRCh38/hg38 17q22-23.1(chr17:59151705-59547602)x3	GDPD1, LINC01476 +20 more	Copy number gain	See cases	GLikely benign
Select item 148363	GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3	AARSD1, AATF +2032 more	Copy number gain	See cases	GPathogenic
Select item 147832	GRCh38/hg38 17q22-23.1(chr17:59151820-59547491)x3	GDPD1, LINC01476 +20 more	Copy number gain	See cases	GBenign
Select item 146320	GRCh38/hg38 17q22-23.1(chr17:59481220-59756756)x1	CLTC, DHX40 +10 more	Copy number loss	See cases	GUncertain significance
Select item 57282	GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3	LOC126862582, LOC126862583 +1753 more	Copy number gain	See cases	GPathogenic

ClinVar