"ISCA site 4"[submitter] AND "HYDIN"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58645	GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3	LOC108281164, LOC109029536 +1426 more	Copy number gain	See cases	GPathogenic
Select item 144332	GRCh38/hg38 16q22.1-24.1(chr16:70414573-84908120)x1	ADAD2, ADAMTS18 +591 more	Copy number loss	See cases	GPathogenic
Select item 149918	GRCh38/hg38 16q22.1-22.2(chr16:70775377-71086235)x1	HYDIN, LOC121587554 +9 more	Copy number loss	See cases	GLikely benign
Select item 149911	GRCh38/hg38 16q22.2(chr16:70873565-71133362)x1	HYDIN, LOC121587554 +3 more	Copy number loss	See cases	GLikely benign
Select item 149910	GRCh38/hg38 16q22.2(chr16:70873565-71133362)x3	HYDIN, LOC121587554 +3 more	Copy number gain	See cases	GLikely benign
Select item 150701	GRCh38/hg38 16q22.2(chr16:70921266-71133362)x3	HYDIN, LOC121587554 +3 more	Copy number gain	See cases	GLikely benign

ClinVar