prkci[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
nsv6291391	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 169,894,343-169,959,222 , GRCh38.p12 chr3: 170,176,555-170,241,434	PRKCI, PHC3
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	PRKCI, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	PRKCI, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	PRKCI, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	PRKCI, LINC02614, 1469 more genes
nsv6637156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502	PRKCI, H1-10, 846 more genes
nsv3918692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833	PRKCI, LOC105374179, 785 more genes
nsv3874894	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426	PRKCI, RNU6-901P, 673 more genes
nsv3918066	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254	PRKCI, LOC105374260, 696 more genes
nsv3918149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383	PRKCI, LINC02031, 647 more genes
nsv3913128	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 156,321,878-198,113,452 , NCBI36 chr3: 157,522,361-199,324,720 , GRCh37 chr3: 156,039,667-197,840,323	PRKCI, SNORA4, 644 more genes
nsv3914686	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 158,493,861-199,345,995 , GRCh37 chr3: 157,011,167-197,861,598 , GRCh38 chr3: 157,293,378-198,134,727	PRKCI, RPL34P10, 625 more genes
nsv3871065	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 158,980,631-197,766,890 , GRCh38.p12 chr3: 159,262,842-198,040,019	PRKCI, LINC02048, 599 more genes
nsv3912173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 167,337,691-199,336,383 , GRCh37 chr3: 165,854,997-197,851,986 , GRCh38 chr3: 166,137,209-198,125,115	PRKCI, LOC105374277, 540 more genes
nsv3918784	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013	PRKCI, LOC105374167, 394 more genes
nsv3918982	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 167,885,356-197,837,049 , NCBI36 chr3: 169,368,050-199,321,446 , GRCh38 chr3: 168,167,568-198,110,178	PRKCI, EIF4G1, 515 more genes
nsv3889215	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 157,128,738-181,637,333 , GRCh38.p12 chr3: 157,410,949-181,919,545	PRKCI, NAALADL2, 274 more genes
nsv4674680	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065	PRKCI, RNU6-1120P, 323 more genes
nsv3913042	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 166,359,093-181,330,650 , GRCh37 chr3: 164,876,399-179,847,956 , GRCh38 chr3: 165,158,611-180,130,168	PRKCI, LOC105374211, 169 more genes
nsv3919833	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 158,141,556-172,788,324 , NCBI36 chr3: 159,342,039-173,988,808 , GRCh37 chr3: 157,859,345-172,506,114	PRKCI, NMD3, 173 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 25

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Number of Variants: 20

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Supplemental Content

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Search details

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