dbVar for OMIM (Select 191041) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7095670	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 55,644,283-55,668,957 , GRCh38.p12 chr19: 55,132,915-55,157,589	DNAAF3, TNNI3, 2 more genes
nsv6310499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 55,652,544-55,656,943 , GRCh38.p12 chr19: 55,141,176-55,145,575	TNNT1
nsv4454487	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 55,140,873-55,147,167 , GRCh37 chr19: 55,652,241-55,658,535	TNNT1
nsv4452266	copy number variation	2	nstd102	human	Uncertain significance	GRCh38 chr19: 55,132,905-55,256,909 , GRCh37 chr19: 55,644,273-55,768,277	DNAAF3, MIR6802, 9 more genes
nsv4451628	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 55,652,231-55,663,305 , GRCh38 chr19: 55,140,863-55,151,937	TNNI3, TNNT1
nsv4349152	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 55,652,193-55,665,240 , GRCh38.p12 chr19: 55,140,825-55,153,872	TNNI3, TNNT1
nsv3877803	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 55,140,863-55,141,322 , GRCh37 chr19: 55,652,231-55,652,690	TNNT1
nsv3870480	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 55,652,231-55,658,545 , GRCh38 chr19: 55,140,863-55,147,177	TNNT1

dbVar