dbVar for Gene (Select 2969) - 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
nsv7040201	inversion	1	nstd229	human		GRCh38 chr7: 74,500,956-74,720,341 , GRCh37.p13 chr7: 73,915,286-74,134,660 , GRCh37.p13 chr7\|NW_003871064.1: 2,030,192-2,249,577	GTF2I-AS1, WBSCR23, 3 more genes
nsv6828809	copy number variation	1	nstd229	human		GRCh38 chr7: 74,594,034-74,726,364 , GRCh37.p13 chr7: 74,008,361-74,140,698 , GRCh37.p13 chr7\|NW_003871064.1: 2,123,270-2,255,600	GTF2IRD1, MIR10525, 2 more genes
nsv6827920	copy number variation	1	nstd229	human		GRCh38 chr7: 74,663,457-74,665,965 , GRCh37.p13 chr7: 74,077,789-74,080,297 , GRCh37.p13 chr7\|NW_003871064.1: 2,192,693-2,195,201	GTF2I
nsv6819653	copy number variation	1	nstd229	human		GRCh38 chr7: 74,722,701-74,724,500 , GRCh37.p13 chr7\|NW_003871064.1: 2,251,937-2,253,736 , GRCh37.p13 chr7: 74,137,021-74,138,833	GTF2I-AS1, GTF2I
nsv6819270	copy number variation	1	nstd229	human		GRCh38 chr7: 74,691,482-74,692,187 , GRCh37.p13 chr7\|NW_003871064.1: 2,220,718-2,221,423 , GRCh37.p13 chr7: 74,105,814-74,106,519	GTF2I-AS1, GTF2I
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
nsv6636910	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,718,278-74,143,060 , GRCh38.p12 chr7: 73,304,281-74,728,722	RNU6-1080P, ELN-AS1, 36 more genes
nsv6636745	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,718,278-74,143,240 , GRCh38.p12 chr7: 73,304,281-74,728,902	CLDN3, METTL27, 36 more genes
nsv6636602	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,643,632-74,143,060 , GRCh38.p12 chr7: 73,229,598-74,728,722	FZD9, WBSCR23, 39 more genes
nsv6636473	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,654,782-74,142,190 , GRCh38.p12 chr7: 73,240,749-74,727,852	ELN-AS1, FKBP6, 38 more genes
nsv6634332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635	RRBP1P1, SLC29A4P1, 2680 more genes
nsv6614934	copy number variation	1	nstd223	human		GRCh38 chr7: 74,663,456-74,665,965 , GRCh37.p13 chr7: 74,077,788-74,080,297 , GRCh37.p13 chr7\|NW_003871064.1: 2,192,692-2,195,201	GTF2I
nsv6614862	copy number variation	1	nstd223	human		GRCh38 chr7: 74,673,101-74,675,000 , GRCh37.p13 chr7: 74,087,425-74,089,324 , GRCh37.p13 chr7\|NW_003871064.1: 2,202,337-2,204,236	GTF2I
nsv6575330	inversion	1	nstd223	human		GRCh38 chr7: 74,689,715-74,690,188 , GRCh37.p13 chr7\|NW_003871064.1: 2,218,951-2,219,424 , GRCh37.p13 chr7: 74,104,049-74,104,522	GTF2I-AS1, GTF2I

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 589

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Number of Variants: 20

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