LOC129390922[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 57282	GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3	LOC126862582, LOC126862583 +1753 more	Copy number gain	See cases	GPathogenic
Select item 149337	GRCh38/hg38 17q24.2(chr17:67584224-68639875)x1	AMZ2, ARSG +62 more	Copy number loss	See cases	GPathogenic
Select item 59609	GRCh38/hg38 17q24.2-24.3(chr17:67833866-70085854)x1	ABCA10, ABCA5 +85 more	Copy number loss	See cases	GPathogenic
Select item 145072	GRCh38/hg38 17q24.2(chr17:67994397-68079905)x1	C17orf58, KPNA2 +4 more	Copy number loss	See cases	GLikely benign
Select item 145071	GRCh38/hg38 17q24.2(chr17:67994397-68079905)x4	C17orf58, KPNA2 +4 more	Copy number gain	See cases	GBenign
Select item 145070	GRCh38/hg38 17q24.2(chr17:67994397-68079905)x3	C17orf58, KPNA2 +4 more	Copy number gain	See cases	GBenign/Likely benign
Select item 145873	GRCh38/hg38 17q24.2(chr17:68041106-68127623)x3	KPNA2, LINC00674 +2 more	Copy number gain	See cases	GLikely benign

ClinVar