dbVar for Gene (Select 283232) - 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
nsv7137204	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 268,586-748,873 , GRCh38.p12 chr11: 268,586-748,873	PKP3, RN7SL838P, 32 more genes
nsv7094013	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 694,739-695,047 , GRCh38.p12 chr11: 694,739-695,047	DEAF1, TMEM80
nsv7093930	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 644,550-795,006 , GRCh38.p12 chr11: 644,550-795,006	LOC105376509, GATD1, 7 more genes
nsv7093693	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,636-819,925 , GRCh38.p12 chr11: 532,636-819,925 , GRCh38.p12 chr11\|NT_187586.1: 62,277-209,248	HRAS, LRRC56, 25 more genes
nsv7068164	inversion	1	nstd229	human		GRCh38 chr11: 525,138-982,890 , GRCh37.p13 chr11: 525,138-982,890	DRD4, LMNTD2-AS1, 32 more genes
nsv7067944	inversion	1	nstd229	human		GRCh38 chr11: 288,558-695,861 , GRCh37.p13 chr11: 288,558-695,861	IRF7, TMEM80, 28 more genes
nsv6895084	copy number variation	1	nstd229	human		GRCh38 chr11: 697,537-703,716 , GRCh37.p13 chr11: 697,537-703,716	TMEM80, DEAF1
nsv6889798	copy number variation	1	nstd229	human		GRCh38 chr11: 694,701-722,900 , GRCh37.p13 chr11: 694,701-722,900	TMEM80, EPS8L2, 1 more genes
nsv6885412	copy number variation	1	nstd229	human		GRCh38 chr11: 701,651-701,768 , GRCh37.p13 chr11: 701,651-701,768	DEAF1, TMEM80
nsv6880816	copy number variation	1	nstd229	human		GRCh38 chr11: 694,601-1,110,400 , GRCh37.p13 chr11: 694,601-1,104,308	TALDO1, CD151, 23 more genes
nsv6637864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177	PNPLA2, OR52H1, 372 more genes
nsv6637212	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 461,373-2,157,956 , GRCh38.p12 chr11: 461,373-2,136,726	MIR6744, PTDSS2, 80 more genes
nsv6634327	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927	SNORA54, PIDD1, 219 more genes
nsv6591624	inversion	1	nstd223	human		GRCh38 chr11: 428,014-744,559 , GRCh37.p13 chr11: 428,014-744,559	MIR210HG, EPS8L2, 20 more genes
nsv6588565	inversion	1	nstd223	human		GRCh38 chr11: 427,925-744,841 , GRCh37.p13 chr11: 427,925-744,841	LOC143666, DEAF1, 20 more genes
nsv6450007	copy number variation	1	nstd223	human		GRCh38 chr11: 642,551-894,924 , GRCh37.p13 chr11: 642,551-894,924	PANO1, SLC25A22, 17 more genes
nsv6444976	copy number variation	1	nstd223	human		GRCh38 chr11: 511,139-740,410 , GRCh37.p13 chr11: 511,139-740,410	LMNTD2-AS1, DRD4, 15 more genes
nsv6442745	copy number variation	1	nstd223	human		GRCh38 chr11: 699,104-843,498 , GRCh37.p13 chr11: 699,104-843,498	TMEM80, PNPLA2, 16 more genes
nsv6315535	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599	OR52Q1P, RNU6-593P, 630 more genes
nsv6309282	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 678,674-838,192 , GRCh38.p12 chr11: 678,674-838,192	CRACR2B, PNPLA2, 15 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 227

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Number of Variants: 20

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