dbVar for Gene (Select 7461) - 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
nsv7137207	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,718,277-74,142,256 , GRCh38.p12 chr7: 73,304,280-74,727,918	ELN-AS1, CLIP2, 36 more genes
nsv7137203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,664,461-74,162,586 , GRCh38.p12 chr7: 73,250,429-74,748,249	VPS37D, ABHD11, 39 more genes
nsv7137102	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,717,395-74,173,168 , GRCh38.p12 chr7: 73,303,398-74,758,838	MIR10525, MIR590, 38 more genes
nsv7137028	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 73,214,501-74,773,500 , GRCh37.p13 chr7\|NW_003871064.1: 743,737-2,302,736 , GRCh37.p13 chr7: 72,631,166-74,187,847	LOC105375350, NSUN5, 41 more genes
nsv7098945	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 73,229,597-74,727,852 , GRCh37.p13 chr7\|NW_003871064.1: 758,833-2,257,088 , GRCh37.p13 chr7: 72,643,631-74,142,190	DNAJC30, MIR10525, 39 more genes
nsv7053887	inversion	1	nstd229	human		GRCh38 chr7: 74,171,934-74,839,189 , GRCh37.p13 chr7\|NW_003871064.1: 1,701,170-2,368,425 , GRCh37.p13 chr7: 73,586,264-74,223,814	LOC107986742, GTF2IRD1, 13 more genes
nsv7053700	inversion	1	nstd229	human		GRCh38 chr7: 74,375,310-74,378,100 , GRCh37.p13 chr7: 73,789,640-73,792,430 , GRCh37.p13 chr7\|NW_003871064.1: 1,904,546-1,907,336	CLIP2
nsv7046658	inversion	1	nstd229	human		GRCh38 chr7: 74,375,266-74,378,029 , GRCh37.p13 chr7: 73,789,596-73,792,359 , GRCh37.p13 chr7\|NW_003871064.1: 1,904,502-1,907,265	CLIP2
nsv6836776	copy number variation	1	nstd229	human		GRCh38 chr7: 74,298,410-74,301,920 , GRCh37.p13 chr7\|NW_003871064.1: 1,827,646-1,831,156 , GRCh37.p13 chr7: 73,712,740-73,716,250	CLIP2
nsv6836128	copy number variation	1	nstd229	human		GRCh38 chr7: 74,313,085-74,315,015 , GRCh37.p13 chr7\|NW_003871064.1: 1,842,321-1,844,251 , GRCh37.p13 chr7: 73,727,415-73,729,345	CLIP2
nsv6834984	copy number variation	1	nstd229	human		GRCh38 chr7: 74,339,901-74,350,500 , GRCh37.p13 chr7: 73,754,231-73,764,830 , GRCh37.p13 chr7\|NW_003871064.1: 1,869,137-1,879,736	CLIP2
nsv6828506	copy number variation	1	nstd229	human		GRCh38 chr7: 74,302,529-74,302,561 , GRCh37.p13 chr7\|NW_003871064.1: 1,831,765-1,831,797 , GRCh37.p13 chr7: 73,716,859-73,716,891	CLIP2
nsv6826547	copy number variation	1	nstd229	human		GRCh38 chr7: 74,320,161-74,324,875 , GRCh37.p13 chr7\|NW_003871064.1: 1,849,397-1,854,111 , GRCh37.p13 chr7: 73,734,491-73,739,205	CLIP2
nsv6824392	copy number variation	1	nstd229	human		GRCh38 chr7: 74,400,978-74,401,244 , GRCh37.p13 chr7\|NW_003871064.1: 1,930,214-1,930,480 , GRCh37.p13 chr7: 73,815,308-73,815,574	CLIP2
nsv6824102	copy number variation	1	nstd229	human		GRCh38 chr7: 74,330,400-74,333,463 , GRCh37.p13 chr7: 73,744,730-73,747,793 , GRCh37.p13 chr7\|NW_003871064.1: 1,859,636-1,862,699	CLIP2
nsv6823940	copy number variation	1	nstd229	human		GRCh38 chr7: 74,295,000-74,324,060 , GRCh37.p13 chr7: 73,709,330-73,738,390 , GRCh37.p13 chr7\|NW_003871064.1: 1,824,236-1,853,296	CLIP2
nsv6820009	copy number variation	1	nstd229	human		GRCh38 chr7: 74,309,655-74,312,363 , GRCh37.p13 chr7: 73,723,985-73,726,693 , GRCh37.p13 chr7\|NW_003871064.1: 1,838,891-1,841,599	CLIP2
nsv6819331	copy number variation	1	nstd229	human		GRCh38 chr7: 74,399,349-74,412,435 , GRCh37.p13 chr7: 73,813,679-73,826,765 , GRCh37.p13 chr7\|NW_003871064.1: 1,928,585-1,941,671	CLIP2
nsv6818261	copy number variation	1	nstd229	human		GRCh38 chr7: 74,294,887-74,298,388 , GRCh37.p13 chr7\|NW_003871064.1: 1,824,123-1,827,624 , GRCh37.p13 chr7: 73,709,217-73,712,718	CLIP2
nsv6636936	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,718,278-74,142,256 , GRCh38.p12 chr7: 73,304,281-74,727,918	ELN-AS1, FKBP6, 36 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Links from Gene

Items: 1 to 20 of 700

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Number of Variants: 20

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