dbVar for OMIM (Select 167000) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5980373	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 108,098,332-108,236,255 , GRCh38.p12 chr11: 108,227,605-108,365,528	C11orf65, ATM
nsv4435814	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 58,705,436-58,742,073 , GRCh37.p13 chr17: 56,782,797-56,819,434	LOC105371843, RAD51C
nsv3170354	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr3: 41,240,915-41,281,944 , GRCh38.p12 chr3: 41,199,424-41,240,453	CTNNB1