plekhg1[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
nsv3893503	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 150,981,044-151,304,777 , GRCh38.p12 chr6: 150,659,908-150,983,641	PLEKHG1, PDCL3P5, 3 more genes
nsv3908667	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 151,145,278-151,199,071 , GRCh38.p12 chr6: 150,824,142-150,877,935	PLEKHG1, MTHFD1L, 1 more genes
nsv4675990	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 150,665,650-151,126,443 , GRCh38.p12 chr6: 150,344,514-150,805,307	PLEKHG1, SSR1P1, 2 more genes
nsv3916405	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 150,744,068-159,894,974 , GRCh38 chr6: 150,381,239-159,553,952 , GRCh37 chr6: 150,702,375-159,974,984	PLEKHG1, LOC112267968, 126 more genes
nsv3890752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 144,075,695-152,337,005 , GRCh38.p12 chr6: 143,754,558-152,015,870	PLEKHG1, LOC105378052, 109 more genes
nsv3920651	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 144,932,561-152,985,364 , NCBI36 chr6: 145,295,390-153,348,192 , GRCh37 chr6: 145,253,697-153,306,499	PLEKHG1, PPP1R14C, 107 more genes
nsv3910985	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 146,843,948-151,790,457 , GRCh37 chr6: 146,802,255-151,748,764 , GRCh38 chr6: 146,481,119-151,427,629	PLEKHG1, RMND1, 77 more genes
nsv4675234	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929	PLEKHG1, RNU7-3P, 86 more genes
nsv3918368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 148,126,255-151,214,851 , GRCh38 chr6: 147,805,119-150,893,715 , NCBI36 chr6: 148,167,948-151,256,544	PLEKHG1, CYP51A1P3, 52 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	PLEKHG1, 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	PLEKHG1, 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	PLEKHG1, 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	PLEKHG1, ITPR3, 2905 more genes
nsv3911993	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033	PLEKHG1, LOC105369171, 418 more genes
nsv3915150	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038	PLEKHG1, KATNA1, 422 more genes
nsv3920975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591	PLEKHG1, UST-AS2, 394 more genes
nsv3908622	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 150,284,435-170,919,470 , GRCh38.p12 chr6: 149,963,299-170,610,382	PLEKHG1, LOC105378120, 319 more genes
nsv3911164	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117	PLEKHG1, HYMAI, 263 more genes
nsv4456488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222	PLEKHG1, PDCL3P5, 176 more genes
nsv4455110	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 151,125,814-151,676,908 , GRCh38.p12 chr6: 150,804,678-151,355,773	PLEKHG1, ARL4AP5, 12 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 21

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Number of Variants: 20

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Supplemental Content

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Search details

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