ClinVar for Gene (Select 126859744) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155438	GRCh38/hg38 6q14.1-16.1(chr6:75926199-92710793)x1	ME1, MEI4 +299 more	Copy number loss	See cases	GPathogenic
Select item 153749	GRCh38/hg38 6q15(chr6:89339079-92096042)x3	ANKRD6, BACH2 +60 more	Copy number gain	See cases	GUncertain significance
Select item 151600	GRCh38/hg38 6q15-16.1(chr6:90687494-93806515)x1	CASC6, EPHA7 +15 more	Copy number loss	See cases	GPathogenic
Select item 150937	GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3	LOC123775388, LOC123775389 +1449 more	Copy number gain	See cases	GPathogenic
Select item 147861	GRCh38/hg38 6q15-16.1(chr6:90888950-93582834)x1	CASC6, EPHA7 +14 more	Copy number loss	See cases	GUncertain significance
Select item 146487	GRCh38/hg38 6q14.2-16.1(chr6:83838303-98822313)x1	SMIM8, SNHG5 +247 more	Copy number loss	See cases	GPathogenic
Select item 146127	GRCh38/hg38 6q14.3-16.1(chr6:85804273-93189258)x1	AKIRIN2, ANKRD6 +153 more	Copy number loss	See cases	GPathogenic
Select item 144893	GRCh38/hg38 6q15(chr6:89931798-91707636)x3	BACH2, CASC6 +33 more	Copy number gain	See cases	GUncertain significance
Select item 58438	GRCh38/hg38 6q14.1-16.1(chr6:82569098-93753476)x1	AKIRIN2, ANKRD6 +220 more	Copy number loss	See cases	GPathogenic

ClinVar