gpr65[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
nsv6314049	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 88,429,733-88,503,392 , GRCh38.p12 chr14: 87,963,389-88,037,048	GPR65, GALC, 3 more genes
nsv4456664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 77,274,990-89,803,137 , GRCh38.p12 chr14: 76,808,647-89,336,793	GPR65, DYNLL1P2, 126 more genes
nsv3893892	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 84,783,137-96,908,198 , GRCh38.p12 chr14: 84,316,793-96,441,861	GPR65, DICER1, 175 more genes
nsv4675107	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153	GPR65, SHLD2P2, 175 more genes
nsv6314190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 88,345,625-94,773,741 , GRCh38.p12 chr14: 87,879,281-94,140,555	GPR65, EML5, 104 more genes
nsv7137135	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 88,401,076-94,725,706 , GRCh38.p12 chr14: 87,934,732-94,140,555	GPR65, LOC100128939, 104 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	GPR65, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	GPR65, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	GPR65, LOC100289511, 1996 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	GPR65, DHRS7, 1946 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	GPR65, SRMP2, 1929 more genes
nsv3904265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229	GPR65, CRIP1, 1929 more genes
nsv3917422	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478	GPR65, MIR656, 1918 more genes
nsv6315524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013	GPR65, PAPOLA-DT, 1338 more genes
nsv3898512	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 73,750,741-107,285,437 , GRCh38.p12 chr14: 73,284,033-106,877,229	GPR65, MEG3, 860 more genes
nsv3922094	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 73,655,772-106,879,298 , GRCh37 chr14: 74,122,475-107,287,505 , NCBI36 chr14: 73,192,228-106,358,550	GPR65, LOC105370614, 849 more genes
nsv3915681	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 76,758,891-106,358,550 , GRCh37 chr14: 77,689,138-107,287,505 , GRCh38 chr14: 77,222,795-106,879,298	GPR65, IGHV3-32, 751 more genes
nsv6637825	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229	GPR65, CHGA, 676 more genes
nsv3914983	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 86,094,030-106,832,642 , GRCh37 chr14: 86,560,374-107,240,869 , NCBI36 chr14: 85,630,127-106,311,914	GPR65, IGHD5-5, 658 more genes
nsv6637462	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 81,593,708-97,059,276 , GRCh38.p12 chr14: 81,127,364-96,592,939	GPR65, SERPINA3, 210 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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