LOC110121211[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58118	GRCh38/hg38 5q32-35.3(chr5:149714592-181272151)x3	ADAM19, ADAMTS2 +1166 more	Copy number gain	See cases	GPathogenic
Select item 144365	GRCh38/hg38 5q33.3-35.3(chr5:156825512-181269805)x3	LOC129995188, LOC129995189 +863 more	Copy number gain	See cases	GPathogenic
Select item 146233	GRCh38/hg38 5q34-35.3(chr5:164386701-181269805)x3	LOC129995377, LOC129995378 +676 more	Copy number gain	See cases	GPathogenic
Select item 152731	GRCh38/hg38 5q35.1-35.3(chr5:169334755-181285301)x3	ADAMTS2, ARL10 +622 more	Copy number gain	See cases	GPathogenic
Select item 2517378	NM_004417.4(DUSP1):c.179T>C (p.Met60Thr)	DUSP1, LOC110121211 (M60T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287717	NM_004417.4(DUSP1):c.175G>T (p.Ala59Ser)	DUSP1, LOC110121211 (A59S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar