pln[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
nsv4450565	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh38 chr6: 118,548,061-118,559,090 , GRCh37 chr6: 118,869,224-118,880,253	PLN, CEP85L
nsv6312021	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr6: 118,880,085-118,880,243 , GRCh38.p12 chr6: 118,558,922-118,559,080	PLN, CEP85L
nsv5564352	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 118,868,442-118,882,587 , GRCh38.p12 chr6: 118,547,279-118,561,424	PLN, CEP85L
nsv3883594	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 118,548,219-118,559,100 , GRCh37 chr6: 118,869,382-118,880,263	PLN, CEP85L
nsv3886556	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 118,558,825-118,560,424 , GRCh37 chr6: 118,879,988-118,881,587	PLN, CEP85L
nsv5381524	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 118,879,986-118,880,253 , GRCh38.p12 chr6: 118,558,823-118,559,090	PLN, CEP85L
nsv4729205	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 118,871,813-119,007,889 , GRCh38.p12 chr6: 118,550,650-118,686,726	PLN, CEP85L, 2 more genes
nsv4729342	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 118,842,806-119,061,150 , GRCh38.p12 chr6: 118,521,643-118,739,987	PLN, LOC107986524, 2 more genes
nsv3914778	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 118,825,150-118,976,065 , GRCh37.p13 chr6: 118,718,457-118,869,372 , GRCh38.p12 chr6: 118,397,294-118,548,209	PLN, CEP85L, 3 more genes
nsv3875226	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 118,823,423-118,880,554 , GRCh38.p12 chr6: 118,502,260-118,559,391	PLN, CEP85L, 1 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	PLN, LOC107986534, 426 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	PLN, 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	PLN, SSXP10, 298 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	PLN, 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	PLN, LOC105377979, 266 more genes
nsv6315321	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791	PLN, SLC18B1, 223 more genes
nsv7148249	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322	PLN, TRDN-AS1, 179 more genes
nsv3924661	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 115,601,230-128,514,324 , GRCh37 chr6: 115,922,394-128,835,469 , NCBI36 chr6: 116,029,087-128,877,162	PLN, MCM9, 146 more genes
nsv4457007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 110,981,075-119,608,396 , GRCh38.p12 chr6: 110,659,872-119,287,231	PLN, HDAC2-AS2, 134 more genes
nsv3918326	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 116,145,074-123,993,898 , GRCh37.p13 chr6: 116,038,381-123,952,199 , GRCh38.p12 chr6: 115,717,217-123,631,054	PLN, MCM9, 93 more genes

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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 50

Page of 3

Number of Variants: 20

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Supplemental Content

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