VPS13C-DT[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57882	GRCh38/hg38 15q21.3-22.2(chr15:57567950-63019415)x1	ADAM10, ALDH1A2 +163 more	Copy number loss	See cases	GPathogenic
Select item 154848	GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	LOC130057806, LOC130057807 +1763 more	Copy number gain	See cases	GPathogenic
Select item 996951	NC_000015.10:g.61919523_62253599dup	C2CD4A, C2CD4B +11 more	Duplication	See cases	GUncertain significance
Select item 1264379	NR_135690.1(VPS13C-DT):n.142C>T	LOC130057212, VPS13C +1 more	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign

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