dbVar for OMIM (Select 192600) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5564319	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 236,906,227-236,906,228 , GRCh38 chr1: 236,742,927-236,742,928	ACTN2
nsv5381293	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 236,848,754-236,928,931 , GRCh38.p12 chr1: 236,685,454-236,765,631	ACTN2
nsv5381069	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr1: 236,849,954-237,551,503 , GRCh38.p12 chr1: 236,686,654-237,388,203	RPL35P1, MTR, 7 more genes
nsv5381030	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 37,821,603-37,822,372 , GRCh38.p12 chr17: 39,665,350-39,666,119	TCAP, PNMT
nsv4682479	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 236,898,925-236,902,842 , GRCh38 chr1: 236,735,625-236,739,542	ACTN2
nsv3889101	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr1: 236,751,450-236,762,639 , GRCh37 chr1: 236,914,750-236,925,939	ACTN2
nsv3879425	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 236,849,954-237,205,889 , GRCh38 chr1: 236,686,654-237,042,589	LOC105373218, RPSAP21, 6 more genes
nsv3872144	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 236,849,954-236,899,988 , GRCh38.p12 chr1: 236,686,654-236,736,688	ACTN2

dbVar