C2675891[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 625818	GRCh37/hg19 1q21.1-21.2(chr1:145740598-147825678)	NBPF12, PDZK1 +10 more	Copy number gain	Chromosome 1q21.1 duplication syndrome	GPathogenic
Select item 625538	GRCh37/hg19 1q21.1-21.2(chr1:145765424-147142037)	ACP6, BCL9 +6 more	Copy number gain	Chromosome 1q21.1 duplication syndrome	GPathogenic
Select item 625537	GRCh37/hg19 1q21.1-21.2(chr1:145103956-147220326)	ACP6, ANKRD34A +23 more	Copy number gain	Chromosome 1q21.1 duplication syndrome	GPathogenic
Select item 625536	GRCh37/hg19 1q21.1-21.2(chr1:145015937-147416122)	ACP6, ANKRD34A +27 more	Copy number gain	Chromosome 1q21.1 duplication syndrome	GPathogenic

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