lpar6[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
nsv5672652	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 48,985,727-49,039,514 , GRCh38.p12 chr13: 48,411,591-48,465,378	LPAR6, RB1
nsv4681305	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 48,953,710-49,054,207 , GRCh38.p12 chr13: 48,379,574-48,480,071	LPAR6, RB1, 1 more genes
nsv4682531	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 48,876,883-49,057,026 , GRCh38.p12 chr13: 48,302,747-48,482,890	LPAR6, RB1, 4 more genes
nsv4681759	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 48,877,837-49,054,207 , GRCh38.p12 chr13: 48,303,701-48,480,071	LPAR6, RB1, 4 more genes
nsv5672727	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 48,877,851-49,054,207 , GRCh38.p12 chr13: 48,303,715-48,480,071	LPAR6, RB1, 4 more genes
nsv3885954	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 48,878,039-49,054,217 , GRCh38 chr13: 48,303,903-48,480,081	LPAR6, RB1, 4 more genes
nsv3877998	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 48,878,043-49,054,213 , GRCh38 chr13: 48,303,907-48,480,077	LPAR6, RB1, 4 more genes
nsv4681688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 48,877,837-48,987,032 , GRCh38.p12 chr13: 48,303,701-48,412,896	LPAR6, RB1, 4 more genes
nsv997203	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr13: 48,303,747-48,481,890 , GRCh37 chr13: 48,877,883-49,056,026	LPAR6, RB1, 4 more genes
nsv3910270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141	LPAR6, RNU6-71P, 1332 more genes
nsv3924528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908	LPAR6, LOC105370271, 925 more genes
nsv3898603	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 42,457,841-91,796,698 , GRCh38.p12 chr13: 41,883,705-91,144,444	LPAR6, RNY4P30, 575 more genes
nsv3918812	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 44,967,523-92,738,168 , NCBI36 chr13: 44,439,658-92,188,422 , GRCh37 chr13: 45,541,658-93,390,421	LPAR6, SRSF1P1, 541 more genes
nsv6314117	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618	LPAR6, RBM26, 591 more genes
nsv3913649	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 41,143,820-85,137,552 , GRCh37 chr13: 41,717,956-85,711,687 , NCBI36 chr13: 40,615,956-84,609,688	LPAR6, RPL21P108, 539 more genes
nsv3882264	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 46,968,080-87,381,985 , GRCh37.p13 chr13: 47,542,215-88,034,240	LPAR6, ARL11, 428 more genes
nsv3915679	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,271,865-70,046,105 , GRCh38 chr13: 30,697,728-69,471,973 , NCBI36 chr13: 30,169,865-68,944,106	LPAR6, CCDC70, 524 more genes
nsv3915859	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 47,117,587-84,300,935 , GRCh37 chr13: 47,691,722-84,875,070 , NCBI36 chr13: 46,589,723-83,773,071	LPAR6, LOC105370231, 406 more genes
nsv3923911	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921	LPAR6, MLNR, 422 more genes
nsv3907596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,946,120-62,698,217 , GRCh38.p12 chr13: 32,371,983-62,124,084	LPAR6, TPT1, 434 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 69

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Number of Variants: 20

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Supplemental Content

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Search details

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