LOC125316775[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	ABCA10, ADAM11 +2032 more	Copy number gain	See cases	GPathogenic
Select item 57282	GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3	LOC130060795, LOC130060796 +1753 more	Copy number gain	See cases	GPathogenic
Select item 152211	GRCh38/hg38 17q24.1-24.2(chr17:64634771-67686888)x1	APOH, AXIN2 +109 more	Copy number loss	See cases	GPathogenic
Select item 157400	Single allele	LOC112533660, LOC121852945 +7 more	Deletion	Small for gestational age	Gnot provided
Select item 157401	NM_002737.2(PRKCA):c.206-81404_206-10168del	LOC125316774, LOC125316775 +5 more	Deletion	Large for gestational age	Gnot provided
Select item 148350	GRCh38/hg38 17q24.2(chr17:66424178-66746437)x1	LOC121852945, LOC125316774 +9 more	Copy number loss	See cases	GUncertain significance

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