dbVar for Gene (Select 5982) - 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
nsv7143673	insertion	1	nstd232	human		GRCh37.p13 chr7: 73,654,426-73,654,426 , GRCh38.p12 chr7: 74,240,096-74,240,096	RFC2
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
nsv6836908	copy number variation	1	nstd229	human		GRCh38 chr7: 74,245,944-74,246,188 , GRCh37.p13 chr7\|NW_003871064.1: 1,775,180-1,775,424 , GRCh37.p13 chr7: 73,660,274-73,660,518	RFC2
nsv6824421	copy number variation	1	nstd229	human		GRCh38 chr7: 74,234,400-74,239,511 , GRCh37.p13 chr7: 73,648,730-73,653,841 , GRCh37.p13 chr7\|NW_003871064.1: 1,763,636-1,768,747	RFC2
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
nsv6636897	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 73,666,853-73,689,952 , GRCh38.p12 chr7: 74,252,523-74,275,622	RFC2
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
nsv6619912	copy number variation	1	nstd223	human		GRCh38 chr7: 74,216,862-74,274,096 , GRCh37.p13 chr7: 73,631,192-73,688,426 , GRCh37.p13 chr7\|NW_003871064.1: 1,746,098-1,803,332	RFC2, LAT2
nsv6614586	copy number variation	1	nstd223	human		GRCh38 chr7: 74,233,821-74,234,696 , GRCh37.p13 chr7: 73,648,151-73,649,026 , GRCh37.p13 chr7\|NW_003871064.1: 1,763,057-1,763,932	RFC2
nsv6613262	copy number variation	1	nstd223	human		GRCh38 chr7: 74,245,885-74,273,418 , GRCh37.p13 chr7\|NW_003871064.1: 1,775,121-1,802,654 , GRCh37.p13 chr7: 73,660,215-73,687,748	RFC2
nsv6611096	copy number variation	1	nstd223	human		GRCh38 chr7: 74,245,882-74,249,267 , GRCh37.p13 chr7: 73,660,212-73,663,597 , GRCh37.p13 chr7\|NW_003871064.1: 1,775,118-1,778,503	RFC2

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Number of Variants: 20

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Has Clinical Interpretation

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Items: 1 to 20 of 363

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Number of Variants: 20

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