dbVar for OMIM (Select 208400) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7097243	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 178,357,420-178,363,667 , GRCh38.p12 chr4: 177,436,266-177,442,513	AGA-DT, AGA
nsv7096989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 178,351,918-178,357,515 , GRCh38.p12 chr4: 177,430,764-177,436,361	AGA
nsv6312246	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 178,352,862-178,363,529 , GRCh38.p12 chr4: 177,431,708-177,442,375	AGA, AGA-DT
nsv5673742	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 178,363,393-178,363,667 , GRCh38.p12 chr4: 177,442,239-177,442,513	AGA-DT, AGA
nsv4683594	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 178,352,842-178,363,549 , GRCh38.p12 chr4: 177,431,688-177,442,395	AGA-DT, AGA