dbVar for OMIM (Select 605131) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4716480	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 78,152,047-78,188,346 , GRCh37.p13 chr16: 78,185,944-78,222,243	WWOX
nsv4685726	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 78,458,767-78,458,953 , GRCh38.p12 chr16: 78,424,870-78,425,056	WWOX
nsv4675330	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 78,198,080-78,198,186 , GRCh38.p12 chr16: 78,164,183-78,164,289	WWOX
nsv4350375	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 78,143,268-78,154,701 , GRCh38.p12 chr16: 78,109,371-78,120,804	WWOX
nsv4350189	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 78,409,180-78,431,277 , GRCh38.p12 chr16: 78,375,283-78,397,380	WWOX
nsv4349119	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 78,458,774-78,463,512 , GRCh38.p12 chr16: 78,424,877-78,429,615	WWOX
nsv3887105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 78,133,327-78,198,186 , GRCh38 chr16: 78,099,413-78,164,289	WWOX
nsv3877844	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 78,342,602-78,424,602 , GRCh37.p13 chr16: 78,376,499-78,458,499	WWOX, LSM3P5
nsv3870592	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 78,260,521-78,417,344 , GRCh38 chr16: 78,226,624-78,383,447	WWOX, LSM3P5, 1 more genes

dbVar