"GeneDx"[submitter] AND "LOC130059441"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59514	GRCh38/hg38 16q22.1-23.1(chr16:69918076-76723348)x1	AARS1, ADAT1 +295 more	Copy number loss	See cases	GPathogenic
Select item 59515	GRCh38/hg38 16q22.3-23.3(chr16:73049467-82576326)x1	LOC112486211, LOC112486212 +360 more	Copy number loss	See cases	GPathogenic
Select item 60022	GRCh38/hg38 16q23.1(chr16:75485676-75603079)x3	ADAT1, CHST5 +22 more	Copy number gain	See cases	GUncertain significance
Select item 1192994	NC_000016.10:g.75556384G>T	LOC130059441, TMEM231	Single nucleotide variant	not provided	GLikely benign

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