dbVar for OMIM (Select 613881) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5672606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 121,411,178-121,437,012 , GRCh38.p12 chr10: 119,651,666-119,677,500	BAG3
nsv5564284	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 121,429,353-121,429,699 , GRCh38.p12 chr10: 119,669,841-119,670,187	BAG3
nsv5380787	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 121,429,353-121,437,012 , GRCh38.p12 chr10: 119,669,841-119,677,500	BAG3
nsv5380710	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 121,411,168-121,429,709 , GRCh38.p12 chr10: 119,651,656-119,670,197	BAG3
nsv4454453	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 119,676,454-119,677,500 , GRCh37 chr10: 121,435,966-121,437,012	BAG3
nsv3887020	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 121,410,882-121,429,689 , GRCh38 chr10: 119,651,370-119,670,177	BAG3
nsv3884719	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 119,669,831-119,670,197 , GRCh37 chr10: 121,429,343-121,429,709	BAG3
nsv3879576	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 121,411,168-121,436,814 , GRCh38 chr10: 119,651,656-119,677,302	BAG3

dbVar