dbVar for Gene (Select 3665) - 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
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
nsv7068392	inversion	1	nstd229	human		GRCh38 chr11: 260,223-620,051 , GRCh37.p13 chr11: 260,223-620,051	MIR210, LMNTD2-AS1, 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
nsv7058883	inversion	1	nstd229	human		GRCh38 chr11: 499,565-690,606 , GRCh37.p13 chr11: 499,565-690,606	LOC143666, DEAF1, 13 more genes
nsv6884188	copy number variation	1	nstd229	human		GRCh38 chr11: 614,696-616,317 , GRCh37.p13 chr11: 614,696-616,317	CDHR5, IRF7
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
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
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
nsv6314711	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr11: 612,814-612,875 , GRCh37 chr11: 612,814-612,875	IRF7
nsv6314656	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr11: 613,613-613,672 , GRCh37 chr11: 613,613-613,672	IRF7
nsv6309203	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 612,645-644,674 , GRCh38.p12 chr11: 612,645-644,674 , GRCh38.p12 chr11\|NT_187586.1: 142,538-176,554	SCT, IRF7, 4 more genes
nsv6309188	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 216,698-720,766 , GRCh38.p12 chr11: 216,698-720,766	NLRP6, PHRF1, 34 more genes
nsv6309115	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 532,636-695,047 , GRCh38.p12 chr11: 532,636-695,047 , GRCh38.p12 chr11\|NT_187586.1: 62,277-209,248	LOC143666, DEAF1, 13 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

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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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Subject Phenotype Status

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Items: 1 to 20 of 297

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Number of Variants: 20

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