dbVar for OMIM (Select 131100) - dbVar - NCBI

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Items: 10

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4684134	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 64,573,469-64,573,813 , GRCh38 chr11: 64,805,997-64,806,341	MEN1
nsv4683843	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr11: 64,571,806-64,578,188 , GRCh38.p12 chr11: 64,804,334-64,810,716	MEN1
nsv4682796	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr11: 64,577,127-64,578,188 , GRCh38.p12 chr11: 64,809,655-64,810,716	MEN1
nsv4455031	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 64,804,324-64,810,716 , GRCh37 chr11: 64,571,796-64,578,188	MEN1
nsv4453956	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 64,573,385-64,575,394 , GRCh38 chr11: 64,805,913-64,807,922	MEN1
nsv3888989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 64,570,986-64,577,604 , GRCh38 chr11: 64,803,514-64,810,132	MEN1, MAP4K2
nsv3887498	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 64,809,659-64,810,115 , GRCh37 chr11: 64,577,131-64,577,587	MEN1
nsv3882253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 64,570,986-64,572,288 , GRCh38 chr11: 64,803,514-64,804,816	MEN1, MAP4K2
nsv3878800	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 64,570,986-64,572,288 , GRCh38 chr11: 64,803,514-64,804,816	MEN1, MAP4K2
nsv1397900	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr11: 64,570,986-64,578,766 , GRCh38.p12 chr11: 64,803,514-64,811,294	MEN1, MAP4K2

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