LOC101928273[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 147544	GRCh38/hg38 2q14.3-22.1(chr2:123445762-140592538)x1	ACMSD, AMER3 +336 more	Copy number loss	See cases	GPathogenic
Select item 146815	GRCh38/hg38 2q21.3-22.2(chr2:136045480-142845159)x3	CXCR4, HNMT +46 more	Copy number gain	See cases	GPathogenic
Select item 152865	GRCh38/hg38 2q22.1(chr2:136863073-138263550)x3	HNMT, LINC01832 +4 more	Copy number gain	See cases	GLikely benign
Select item 148432	GRCh38/hg38 2q22.1-22.3(chr2:136937358-146681810)x1	ARHGAP15, ARHGAP15-AS1 +75 more	Copy number loss	See cases	GPathogenic
Select item 58904	GRCh38/hg38 2q22.1(chr2:136937358-138263550)x3	HNMT, LINC01832 +4 more	Copy number gain	See cases	GUncertain significance
Select item 155647	GRCh38/hg38 2q22.1(chr2:137433939-138535492)x3	HNMT, LINC01832 +12 more	Copy number gain	See cases	GLikely benign

ClinVar