"GeneDx"[submitter] AND "LOC129992297"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58026	GRCh38/hg38 4p15.33-15.31(chr4:14659764-18274924)x3	BST1, C1QTNF7 +84 more	Copy number gain	See cases	GPathogenic
Select item 1707146	NC_000004.12:g.16226530GCCCC[3]	LOC129992297, TAPT1	Microsatellite (genic upstream transcript variant)	not provided	GLikely benign
Select item 1252499	NC_000004.12:g.16226554GCC[9]	LOC129992297, TAPT1	Microsatellite	not provided	GBenign
Select item 1225651	NC_000004.12:g.16226554GCC[8]	LOC129992297, TAPT1	Microsatellite	not provided	GBenign
Select item 1186277	NC_000004.12:g.16226554GCC[5]	LOC129992297, TAPT1	Microsatellite	not provided	GLikely benign

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