trpc6[All Fields] AND 1[has_clinical] - 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
nsv3906606	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 101,401,444-101,437,288 , GRCh38.p12 chr11: 101,530,713-101,566,557	TRPC6
nsv3905552	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 101,311,359-101,330,090 , GRCh38.p12 chr11: 101,440,628-101,459,359	TRPC6
nsv3900150	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr11: 101,397,368-101,472,351 , GRCh38.p12 chr11: 101,526,637-101,601,620	TRPC6, KIAA1191P2
nsv3918553	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 101,580,685-101,907,935 , GRCh37 chr11: 101,451,416-101,778,666 , NCBI36 chr11: 100,956,626-101,283,876	TRPC6, KIAA1191P2, 2 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	TRPC6, FAUP4, 2031 more genes
nsv3904761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514	TRPC6, RPS6P16, 449 more genes
nsv3913977	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356	TRPC6, PLS1P1, 349 more genes
nsv3910101	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616	TRPC6, PHB1P16, 385 more genes
nsv6637396	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313	TRPC6, LOC107984375, 295 more genes
nsv3894488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 88,152,458-109,414,650 , GRCh38.p12 chr11: 88,419,290-109,543,924	TRPC6, RNU6-16P, 270 more genes
nsv3910663	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308	TRPC6, LOC101060084, 230 more genes
nsv3922508	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037	TRPC6, AMOTL1, 240 more genes
nsv5672640	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976	TRPC6, HSPD1P13, 239 more genes
nsv6637687	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793	TRPC6, GRIA4, 111 more genes
nsv3924464	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 97,733,839-105,435,083 , GRCh38 chr11: 98,357,901-106,059,146 , GRCh37 chr11: 98,228,629-105,929,873	TRPC6, ARHGAP42, 91 more genes
nsv6309019	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 101,323,686-103,349,981 , GRCh38.p12 chr11: 101,452,955-103,479,253	TRPC6, RPL21P96, 40 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	TRPC6, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	TRPC6, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	TRPC6, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	TRPC6, PYGM, 2125 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 31

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Number of Variants: 20

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Search details

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