dbVar for OMIM (Select 613172) - dbVar - NCBI

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Items: 5

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Number of Variants: 5

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4681125	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 112,579,820-112,595,746 , GRCh38.p12 chr10: 110,820,062-110,835,988	RBM20
nsv4455012	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 110,780,791-110,823,624 , GRCh37 chr10: 112,540,549-112,583,382	RBM20
nsv4451102	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 110,780,781-110,835,998 , GRCh37 chr10: 112,540,539-112,595,756	RBM20
nsv3889915	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 112,579,810-112,595,756 , GRCh38 chr10: 110,820,052-110,835,998	RBM20
nsv3871649	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 110,644,435-110,823,634 , GRCh37 chr10: 112,404,193-112,583,392	RNA5SP327, RBM20, 1 more genes

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