dbVar for Gene (Select 55367) - 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
nsv7094186	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702	OR7E117P, RPLP2, 124 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
nsv6894613	copy number variation	1	nstd229	human		GRCh38 chr11: 800,438-800,553 , GRCh37.p13 chr11: 800,438-800,553	PIDD1
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
nsv6591865	inversion	1	nstd223	human		GRCh38 chr11: 744,286-806,476 , GRCh37.p13 chr11: 744,286-806,476	TALDO1, CEND1, 6 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
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
nsv6438165	copy number variation	1	nstd223	human		GRCh38 chr11: 737,066-3,896,161 , GRCh37.p13 chr11: 737,066-3,917,391	RNU6-878P, CARS1-AS1, 123 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
nsv6291427	copy number variation	1	nstd102	human	not provided	GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125	OR52J1P, IFITM1, 255 more genes
nsv6290808	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 648,556-1,021,236 , GRCh38.p12 chr11: 648,556-1,021,236	PIDD1, TSPAN4, 20 more genes
nsv6281571	insertion	1	nstd214	human		GRCh38 chr11: 800,459-800,459 , GRCh37.p13 chr11: 800,459-800,459	PIDD1
nsv6279005	insertion	4	nstd214	human		GRCh38 chr11: 800,486-800,486 , GRCh37.p13 chr11: 800,486-800,486	PIDD1
nsv6272992	copy number variation	1	nstd214	human		GRCh38 chr11: 806,262-806,402 , GRCh37.p13 chr11: 806,262-806,402	PIDD1
nsv6271332	copy number variation	1	nstd214	human		GRCh38 chr11: 801,741-801,792 , GRCh37.p13 chr11: 801,741-801,792	PIDD1

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

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Items: 1 to 20 of 257

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Number of Variants: 20

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