dbVar for OMIM (Select 615249) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7097796	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 42,977,230-43,054,712 , GRCh38.p12 chr8: 43,122,087-43,199,569	POMK, HGSNAT, 1 more genes
nsv6312911	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr8: 42,958,692-43,054,712 , GRCh38.p12 chr8: 43,103,549-43,199,569	POMK, RNY5P6, 1 more genes
nsv6312724	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 42,958,682-42,958,983 , GRCh38.p12 chr8: 43,103,539-43,103,840	POMK
nsv4453018	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 43,103,539-43,103,840 , GRCh37 chr8: 42,958,682-42,958,983	POMK
nsv4452374	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr8: 43,103,539-43,122,887 , GRCh37 chr8: 42,958,682-42,978,030	POMK
nsv4451969	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr8: 42,837,952-43,122,887 , GRCh37 chr8: 42,693,095-42,978,030	MIR4469, RNU1-124P, 6 more genes
nsv3885312	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 42,958,672-42,978,040 , GRCh38.p12 chr8: 43,103,529-43,122,897	POMK

dbVar