"GeneDx"[submitter] AND "TSGA10"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59145	GRCh38/hg38 2p11.2-q11.2(chr2:91443218-102334856)x3	ACTR1B, ADRA2B +331 more	Copy number gain	See cases	GPathogenic
Select item 152537	GRCh38/hg38 2q11.1-13(chr2:94678532-110602409)x3	ACTR1B, ADRA2B +550 more	Copy number gain	See cases	GPathogenic
Select item 59146	GRCh38/hg38 2q11.1-12.1(chr2:94817406-103252396)x3	LOC129934355, LOC129934356 +348 more	Copy number gain	See cases	GPathogenic
Select item 59147	GRCh38/hg38 2q11.2-13(chr2:97672522-110211318)x3	AFF3, C2orf15 +373 more	Copy number gain	See cases	GPathogenic
Select item 1294393	NC_000002.12:g.99154805G>C	LIPT1, TSGA10	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1270802	NC_000002.12:g.99154809C>T	LIPT1, TSGA10	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign

ClinVar