dbVar for OMIM (Select 616878) - dbVar - NCBI

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Items: 4

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Number of Variants: 4

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4716463	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 20,036,383-20,045,781 , GRCh38 chr22: 20,048,860-20,058,258	TANGO2
nsv4685774	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 20,036,384-20,045,784 , GRCh38.p12 chr22: 20,048,861-20,058,261	TANGO2
nsv4685763	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 20,029,135-20,062,954 , GRCh38.p12 chr22: 20,041,612-20,075,431	TANGO2
nsv1398490	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr22: 20,041,612-20,075,431 , GRCh37 chr22: 20,029,135-20,062,954	TANGO2

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