gpr6[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
nsv3912258	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 110,208,809-110,630,205 , GRCh38 chr6: 109,780,913-110,202,309 , GRCh37 chr6: 110,102,116-110,523,512	GPR6, WASF1, 3 more genes
nsv3885190	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 110,080,484-110,472,732 , GRCh38.p12 chr6: 109,759,281-110,151,529	GPR6, WASF1, 2 more genes
nsv6636955	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 110,096,791-110,491,262 , GRCh38.p12 chr6: 109,775,588-110,170,059	GPR6, WASF1, 2 more genes
nsv6636867	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 110,098,753-110,491,262 , GRCh38.p12 chr6: 109,777,550-110,170,059	GPR6, WASF1, 2 more genes
nsv3880626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541	GPR6, LOC107986534, 426 more genes
nsv6313858	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488	GPR6, RN7SL509P, 311 more genes
nsv3924576	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694	GPR6, TUBE1, 318 more genes
nsv3920683	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 109,372,795-132,430,553 , GRCh37 chr6: 109,266,102-132,388,860 , GRCh38 chr6: 108,944,899-132,067,720	GPR6, SSXP10, 298 more genes
nsv3876958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 95,549,951-116,684,929 , GRCh38.p12 chr6: 94,840,233-116,363,766	GPR6, LIN28B-AS1, 258 more genes
nsv3910417	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 100,054,889-120,488,154 , NCBI36 chr6: 100,609,486-120,850,999 , GRCh37 chr6: 100,502,765-120,809,300	GPR6, LINC02518, 266 more genes
nsv3924741	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 106,951,594-126,102,365 , GRCh38 chr6: 106,503,719-125,781,219 , NCBI36 chr6: 107,058,287-126,144,058	GPR6, LOC105377979, 266 more genes
nsv4768376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741	GPR6, LOC101927405, 211 more genes
nsv3919897	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 103,834,033-114,362,096 , GRCh37 chr6: 103,727,340-114,255,403 , GRCh38 chr6: 103,279,465-113,934,239	GPR6, HACE1, 174 more genes
nsv3913170	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 102,911,070-111,477,775 , GRCh38 chr6: 102,356,502-111,049,879 , GRCh37 chr6: 102,804,377-111,371,082	GPR6, RPS19P5, 121 more genes
nsv3914025	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 107,798,038-116,255,339 , GRCh38 chr6: 107,370,141-115,827,482 , GRCh37 chr6: 107,691,345-116,148,646	GPR6, TRAF3IP2-AS1, 139 more genes
nsv3917185	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 107,873,178-110,975,803 , GRCh38 chr6: 107,445,281-110,547,907 , GRCh37 chr6: 107,766,485-110,869,110	GPR6, SMPD2, 56 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	GPR6, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	GPR6, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	GPR6, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	GPR6, ITPR3, 2905 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 27

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Number of Variants: 20

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Supplemental Content

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Search details

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