ClinVar for Gene (Select 148145) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155638	GRCh38/hg38 19q11-13.11(chr19:27780238-34783942)x3	ANKRD27, C19orf12 +210 more	Copy number gain	See cases	GUncertain significance
Select item 153629	GRCh38/hg38 19q12(chr19:28673355-29139775)x1	LINC00906, LINC01532 +2 more	Copy number loss	See cases	GUncertain significance
Select item 152251	GRCh38/hg38 19q12(chr19:28487231-29111075)x1	LINC00906, LINC01532 +7 more	Copy number loss	See cases	GUncertain significance
Select item 146930	GRCh38/hg38 19q12(chr19:28649927-29041050)x1	LINC00906, LINC01532 +3 more	Copy number loss	See cases	GBenign
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic
Select item 57042	GRCh38/hg38 19p13.11-q13.11(chr19:17176767-34924150)x3	LOC130064154, LOC130064155 +625 more	Copy number gain	See cases	GPathogenic

ClinVar