dbVar for Gene (Select 64787) - 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
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
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
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
nsv6887210	copy number variation	1	nstd229	human		GRCh38 chr11: 719,111-742,168 , GRCh37.p13 chr11: 719,111-742,168	EPS8L2, LOC105376509
nsv6883124	copy number variation	1	nstd229	human		GRCh38 chr11: 711,781-712,083 , GRCh37.p13 chr11: 711,781-712,083	EPS8L2
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
nsv6878285	copy number variation	1	nstd229	human		GRCh38 chr11: 712,784-715,907 , GRCh37.p13 chr11: 712,784-715,907	EPS8L2
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
nsv6595242	inversion	1	nstd223	human		GRCh38 chr11: 718,027-718,689 , GRCh37.p13 chr11: 718,027-718,689	EPS8L2
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
nsv6452251	copy number variation	1	nstd223	human		GRCh38 chr11: 715,697-718,843 , GRCh37.p13 chr11: 715,697-718,843	EPS8L2
nsv6452015	copy number variation	1	nstd223	human		GRCh38 chr11: 712,786-715,907 , GRCh37.p13 chr11: 712,786-715,907	EPS8L2
nsv6451853	copy number variation	1	nstd223	human		GRCh38 chr11: 716,546-718,903 , GRCh37.p13 chr11: 716,546-718,903	EPS8L2
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

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Number of Variants: 20

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Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 281

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Number of Variants: 20

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