dbVar for Gene (Select 84865) - 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
nsv7141289	copy number variation	1	nstd232	human		GRCh37.p13 chr2: 74,699,596-74,699,693 , GRCh38.p12 chr2: 74,472,469-74,472,566	CCDC142, MRPL53
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
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
nsv7042648	inversion	1	nstd229	human		GRCh38 chr2: 74,480,812-74,480,824 , GRCh37.p13 chr2: 74,707,939-74,707,951	CCDC142
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
nsv6693990	copy number variation	1	nstd229	human		GRCh38 chr2: 74,462,734-74,473,098 , GRCh37.p13 chr2: 74,689,861-74,700,225	MRPL53, MOGS, 1 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
nsv6683353	copy number variation	1	nstd229	human		GRCh38 chr2: 74,468,501-74,471,000 , GRCh37.p13 chr2: 74,695,628-74,698,127	MRPL53, CCDC142
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
nsv6140128	copy number variation	1	nstd206	human		GRCh38 chr2: 74,451,619-74,475,619 , GRCh37.p13 chr2: 74,678,746-74,702,746	MOGS, WBP1, 4 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
nsv5554214	mobile element insertion	1	nstd206	human		GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595	, POLR1B, 2149 more genes

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 125

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Number of Variants: 20

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