"ISCA Site 6"[submitter] AND "SCNN1B"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 395601	GRCh37/hg19 16p12.3-11.2(chr16:19424115-30142220)x3	ACSM1, ACSM2A +119 more	Copy number gain	See cases	GPathogenic
Select item 395502	GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3	ABCC6, BCL7C +811 more	Copy number gain	See cases	GPathogenic
Select item 394763	GRCh37/hg19 16p12.2(chr16:23291211-23322012)x3	SCNN1B	Copy number gain	See cases	GUncertain significance
Select item 394018	GRCh37/hg19 16p12.2(chr16:23315377-23355254)x3	SCNN1B	Copy number gain	See cases	GLikely benign

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