"Bionano Laboratories"[submitter] AND "SNTG2"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 689229	GRCh37/hg19 2p25.3(chr2:1091420-1231315)x1	SNTG2	Copy number loss	not provided	GUncertain significance
Select item 688828	GRCh37/hg19 2p25.3(chr2:788889-1053456)x3	SNTG2	Copy number gain	not provided	GUncertain significance
Select item 688787	GRCh37/hg19 2p25.3(chr2:788889-1053456)x3	SNTG2	Copy number gain	not provided	GUncertain significance
Select item 688279	GRCh37/hg19 2p25.3(chr2:12770-2348876)x1	ACP1, ALKAL2 +7 more	Copy number loss	not provided	GPathogenic
Select item 687448	GRCh37/hg19 2p25.3(chr2:922539-985369)x1	SNTG2	Copy number loss	not provided	GUncertain significance
Select item 686794	GRCh37/hg19 2p25.3(chr2:1269373-1542297)x3	SNTG2, TPO	Copy number gain	not provided	GUncertain significance
Select item 686793	GRCh37/hg19 2p25.3(chr2:1097715-1231315)x4	SNTG2	Copy number gain	not provided	GUncertain significance
Select item 686589	GRCh37/hg19 2p25.3(chr2:1193606-1315346)x3	SNTG2	Copy number gain	not provided	GUncertain significance
Select item 686579	GRCh37/hg19 2p25.3(chr2:1131015-1345948)x1	SNTG2	Copy number loss	not provided	GUncertain significance
Select item 686549	GRCh37/hg19 2p25.3-25.1(chr2:12770-7502796)x3	ACP1, ADI1 +19 more	Copy number gain	not provided	GPathogenic
Select item 686548	GRCh37/hg19 2p25.3-25.1(chr2:12770-7502796)x3	ACP1, ADI1 +19 more	Copy number gain	not provided	GPathogenic
Select item 686201	GRCh37/hg19 2p25.3(chr2:12770-3819558)x3	ACP1, ADI1 +15 more	Copy number gain	not provided	GUncertain significance
Select item 686001	GRCh37/hg19 2p25.3(chr2:12770-2832894)x1	ACP1, ALKAL2 +7 more	Copy number loss	not provided	GPathogenic
Select item 685303	GRCh37/hg19 2p25.3(chr2:843845-1862481)x3	MYT1L, PXDN +2 more	Copy number gain	not provided	GUncertain significance
Select item 685096	GRCh37/hg19 2p25.3(chr2:776559-1037783)x3	SNTG2	Copy number gain	not provided	GUncertain significance