dbVar for OMIM (Select 192430) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4578297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,661,724-21,505,417 , GRCh38.p12 chr22: 18,178,957-21,151,128	SERPIND1, ESS2, 130 more genes
nsv4436810	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,631,364-21,800,471 , GRCh38.p12 chr22: 18,148,597-21,446,182	FAM230E, RANBP1, 144 more genes
nsv4436806	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,919,477-21,800,471 , GRCh38.p12 chr22: 18,339,130-21,446,182	C22orf39, MIR6816, 139 more genes
nsv4436787	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,912,231-21,465,672 , GRCh38.p12 chr22: 18,339,130-21,111,383	LOC100129254, GGTLC5P, 125 more genes
nsv4436778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,636,749-21,800,471 , GRCh38.p12 chr22: 18,153,982-21,446,182	FAM247A, LOC107985584, 144 more genes
nsv4436770	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,922,151-21,449,911 , GRCh38.p12 chr22: 18,339,130-21,095,622	ZDHHC8, CLDN5, 123 more genes