dbVar for OMIM (Select 605515) - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3881933	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 70,992,485-71,180,270 , GRCh37 chr3: 71,041,636-71,229,421	FOXP1
nsv3877642	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 71,109,689-71,508,061 , GRCh37.p13 chr3: 71,026,999-71,425,371 , GRCh38.p12 chr3: 70,977,848-71,376,220	FOXP1-AS1, FOXP1
nsv997040	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr3: 71,003,865-71,633,140 , GRCh38.p12 chr3: 70,954,714-71,583,989	FOXP1, MIR1284, 1 more genes

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dbVar