dbVar for OMIM (Select 608769) - 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
nsv7098782	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 34,988,362-34,999,670 , GRCh38.p12 chr11: 34,966,815-34,978,123	PDHX
nsv6634608	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 34,953,032-35,006,116 , GRCh38.p12 chr11: 34,931,485-34,984,569	PDHX, MIR1343
nsv4578518	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 34,989,224-34,993,136 , GRCh37 chr11: 35,010,771-35,014,683	PDHX
nsv3883729	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 34,938,280-34,952,952 , GRCh38 chr11: 34,916,733-34,931,405	PDHX, APIP

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