dbVar for OMIM (Select 601962) - 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
nsv7093413	delins	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,281,499-33,281,551 , GRCh38 chr6: 33,313,722-33,313,774	TAPBP, ZBTB22
nsv6312574	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr6: 32,802,911-32,808,844 , GRCh38.p12 chr6: 32,835,134-32,841,067	TAP2, PSMB8
nsv5673673	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,276,772-33,281,549 , GRCh38 chr6: 33,308,995-33,313,772	TAPBP, ZBTB22
nsv5381623	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,269,517-33,269,568 , GRCh38.p12 chr6: 33,301,740-33,301,791	TAPBP

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