dbVar for OMIM (Select 613640) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5380914	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 77,984,371-77,984,520 , GRCh38.p12 chr14: 77,518,028-77,518,177	SPTLC2
nsv5380832	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 77,978,617-77,978,756 , GRCh38.p12 chr14: 77,512,274-77,512,413	SPTLC2
nsv4683183	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 77,978,617-78,045,462 , GRCh38.p12 chr14: 77,512,274-77,579,119	SPTLC2, RN7SL587P
nsv4681773	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 78,082,781-78,082,932 , GRCh38.p12 chr14: 77,616,438-77,616,589	SPTLC2
nsv4453689	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 77,743,699-78,082,942 , GRCh38 chr14: 77,277,356-77,616,599	VIPAS39, AHSA1, 9 more genes
nsv4450832	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 78,045,288-78,045,462 , GRCh38 chr14: 77,578,945-77,579,119	SPTLC2

dbVar