dbVar for Gene (Select 135886) - 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
nsv7054142	inversion	1	nstd229	human		GRCh38 chr7: 73,807,596-73,871,227 , GRCh37.p13 chr7\|NW_003871064.1: 1,336,832-1,400,463 , GRCh37.p13 chr7: 73,221,926-73,285,557	CLDN4, TMEM270, 1 more genes
nsv7053197	inversion	1	nstd229	human		GRCh38 chr7: 72,920,579-74,172,062 , GRCh37.p13 chr7: 72,391,116-73,586,392 , GRCh37.p13 chr7\|NW_003871064.1: 449,815-1,701,298	FKBP6, TRIM74, 41 more genes
nsv6822994	copy number variation	1	nstd229	human		GRCh38 chr7: 73,862,870-73,868,149 , GRCh37.p13 chr7: 73,277,200-73,282,479 , GRCh37.p13 chr7\|NW_003871064.1: 1,392,106-1,397,385	TMEM270
nsv6637056	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 73,193,427-73,434,586 , GRCh38.p12 chr7: 73,779,097-74,020,256	TMEM270, METTL27, 1 more genes
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
nsv6631938	copy number variation	1	nstd224	human		GRCh37 chr7: 73,108,924-73,425,238 , GRCh38.p12 chr7: 73,694,594-74,010,908	CLDN3, ABHD11, 9 more genes
nsv6614161	copy number variation	1	nstd223	human		GRCh38 chr7: 73,861,936-73,862,244 , GRCh37.p13 chr7: 73,276,266-73,276,574 , GRCh37.p13 chr7\|NW_003871064.1: 1,391,172-1,391,480	TMEM270
nsv6574642	inversion	1	nstd223	human		GRCh38 chr7: 72,920,579-74,172,062 , GRCh37.p13 chr7\|NW_003871064.1: 449,815-1,701,298 , GRCh37.p13 chr7: 72,391,116-73,586,392	CLDN4, TBL2, 41 more genes
nsv6315451	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,700,942-74,142,190 , GRCh38.p12 chr7: 73,286,940-74,727,852	STX1A, METTL27, 37 more genes
nsv6315444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,718,123-74,142,190 , GRCh38.p12 chr7: 73,304,126-74,727,852	STX1A, LOC105375350, 36 more genes

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 328

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Number of Variants: 20

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