dbVar for Gene (Select 27429) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7147050	copy number variation	1	nstd232	human		GRCh37.p13 chr2: 74,756,409-74,756,487 , GRCh38.p12 chr2: 74,529,282-74,529,360	AUP1, HTRA2
nsv7145540	copy number variation	1	nstd232	human		GRCh37.p13 chr2: 74,754,965-74,755,065 , GRCh38.p12 chr2: 74,527,838-74,527,938	AUP1, HTRA2
nsv7145381	copy number variation	1	nstd232	human		GRCh37.p13 chr2: 74,754,717-74,754,861 , GRCh38.p12 chr2: 74,527,590-74,527,734	AUP1, HTRA2
nsv7138404	copy number variation	1	nstd232	human		GRCh37.p13 chr2: 74,756,062-74,756,257 , GRCh38.p12 chr2: 74,528,935-74,529,130	AUP1, HTRA2
nsv7098872	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 73,716,761-75,347,894 , GRCh38.p12 chr2: 73,489,634-75,120,768	RTKN, PCGF1, 61 more genes
nsv7096917	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,753,829-74,757,416 , GRCh38.p12 chr2: 74,526,702-74,530,289	AUP1, LOXL3, 2 more genes
nsv7096907	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 72,359,356-74,779,761 , GRCh38.p12 chr2: 72,132,227-74,552,634	RNU6-111P, LOC105374800, 71 more genes
nsv7096902	copy number variation	3	nstd102	human	Pathogenic	GRCh37 chr2: 71,004,499-74,779,761 , GRCh38.p12 chr2: 70,777,367-74,552,634	TAF13P2, LOC107985897, 100 more genes
nsv7096520	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 69,240,632-74,779,761 , GRCh38.p12 chr2: 69,013,500-74,552,634	LOC112268419, DQX1, 140 more genes
nsv7039989	inversion	1	nstd229	human		GRCh38 chr2: 74,303,206-79,264,856 , GRCh37.p13 chr2: 74,530,333-79,491,982	WBP1, DCTN1-AS1, 80 more genes
nsv6686690	copy number variation	1	nstd229	human		GRCh38 chr2: 74,366,401-74,559,400 , GRCh37.p13 chr2: 74,593,528-74,786,527	DCTN1, CCDC142, 21 more genes
nsv6683032	copy number variation	1	nstd229	human		GRCh38 chr2: 74,525,041-74,529,402 , GRCh37.p13 chr2: 74,752,168-74,756,529	AUP1, HTRA2, 1 more genes
nsv6679949	copy number variation	1	nstd229	human		GRCh38 chr2: 74,368,859-74,528,317 , GRCh37.p13 chr2: 74,595,986-74,755,444	LBX2, WBP1, 18 more genes
nsv6658277	copy number variation	1	nstd229	human		GRCh38 chr2: 73,985,401-74,561,400 , GRCh37.p13 chr2: 74,212,528-74,788,527	MOGS, NECAP1P2, 32 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	CYP1B1-AS1, LOC107985771, 1649 more genes
nsv6628141	copy number variation	1	nstd224	human		GRCh37 chr2: 74,058,095-75,146,159 , GRCh38.p12 chr2: 73,830,968-74,919,032	AUP1, DCTN1, 48 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	LOC112268439, RNA5SP116, 3737 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	ACTG2, ACYP2, 1713 more genes
nsv6134545	copy number variation	2	nstd213	human		GRCh37 chr2: 47,990,000-75,070,001 , GRCh38.p12 chr2: 47,762,861-74,842,874	ACTG2, ACYP2, 438 more genes
nsv6134457	copy number variation	1	nstd213	human		GRCh37 chr2: 38,410,000-75,540,001 , GRCh38.p12 chr2: 38,182,858-75,312,875	, ACTG2, 598 more genes

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Number of Variants: 20

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