pcsk6[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
nsv3918014	copy number variation	1	nstd102	human	Benign	GRCh38 chr15: 101,395,679-101,452,091 , GRCh37 chr15: 101,935,884-101,992,296 , NCBI36 chr15: 99,753,407-99,809,819	PCSK6
nsv3891956	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 101,920,286-101,985,814 , GRCh38.p12 chr15: 101,380,081-101,445,609	PCSK6
nsv3899103	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 102,024,136-102,030,606 , GRCh38.p12 chr15: 101,483,931-101,490,403	PCSK6, LOC107987228
nsv3898108	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 102,024,136-102,030,274 , GRCh38.p12 chr15: 101,483,931-101,490,071	PCSK6, LOC107987228
nsv3890354	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 102,025,218-102,030,162 , GRCh38.p12 chr15: 101,485,013-101,489,959	PCSK6, LOC107987228
nsv3893919	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 102,029,228-102,030,606 , GRCh38.p12 chr15: 101,489,023-101,490,403	PCSK6, LOC107987228
nsv3904263	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 102,029,228-102,030,496 , GRCh38.p12 chr15: 101,489,023-101,490,293	PCSK6, LOC107987228
nsv3909269	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 101,932,462-102,094,078 , GRCh38.p12 chr15: 101,392,257-101,553,875	PCSK6, LOC107987228
nsv4675853	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr15: 101,821,632-101,951,752 , GRCh38.p12 chr15: 101,281,427-101,411,547	PCSK6, SNRPA1, 2 more genes
nsv3904691	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 101,936,157-102,157,749 , GRCh38.p12 chr15: 101,395,952-101,617,546	PCSK6, LINC02348, 2 more genes
nsv3901378	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 101,948,212-102,147,139 , GRCh38.p12 chr15: 101,408,007-101,606,936	PCSK6, SNRPCP18, 2 more genes
nsv3909253	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 101,944,959-102,143,080 , GRCh38.p12 chr15: 101,404,754-101,602,877	PCSK6, LOC107987228, 2 more genes
nsv3910549	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr15: 99,815,580-99,961,672 , GRCh37 chr15: 101,998,057-102,144,149 , GRCh38 chr15: 101,457,852-101,603,946	PCSK6, SNRPCP18, 2 more genes
nsv6291506	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 101,822,986-101,856,106 , GRCh38.p12 chr15: 101,282,781-101,315,901	PCSK6, LOC100507472, 1 more genes
nsv3918091	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 99,753,347-99,935,183 , GRCh37.p13 chr15: 101,935,824-102,117,660 , GRCh38.p12 chr15: 101,395,619-101,577,457	PCSK6, LOC107987228, 1 more genes
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	PCSK6, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	PCSK6, RNU6-18P, 1442 more genes
nsv4729092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189	PCSK6, CHD2, 272 more genes
nsv4675149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909	PCSK6, TTLL13, 264 more genes
nsv3908429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 90,346,994-102,354,798 , GRCh38.p12 chr15: 89,803,763-101,814,595	PCSK6, RPL31P55, 201 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 127

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Number of Variants: 20

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