cyp2c9[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
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	CYP2C9, RNU7-12P, 1876 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	CYP2C9, EIF2S2P3, 895 more genes
nsv3911437	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 93,181,201-101,356,779 , NCBI36 chr10: 94,930,948-103,106,526 , GRCh37 chr10: 94,940,958-103,116,536	CYP2C9, SLF2, 171 more genes
nsv3894877	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,908,171-101,809,723 , GRCh38.p12 chr10: 92,148,414-100,049,966	CYP2C9, RNY3P12, 146 more genes
nsv3908115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 92,667,881-98,970,384 , GRCh38.p12 chr10: 90,908,124-97,210,627	CYP2C9, EXOC6, 118 more genes
nsv3912487	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,386,437-99,514,859 , GRCh38 chr10: 92,626,680-97,755,102 , NCBI36 chr10: 94,376,417-99,504,849	CYP2C9, ENTPD1-AS1, 105 more genes
nsv7098887	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213	CYP2C9, LGI1, 79 more genes
nsv3914138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,403,676-97,230,894 , GRCh38 chr10: 92,643,919-95,471,137 , NCBI36 chr10: 94,393,656-97,220,884	CYP2C9, RPL7AP52, 51 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	CYP2C9, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	CYP2C9, AGAP14P, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	CYP2C9, ANXA11, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	CYP2C9, TUBB8, 2085 more genes
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	CYP2C9, EXOC6, 1906 more genes
nsv3905489	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639	CYP2C9, LOC105378476, 688 more genes
nsv3890046	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,346,520-135,427,143 , GRCh38.p12 chr10: 92,586,763-133,613,639	CYP2C9, UROS, 667 more genes
nsv4348834	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 94,393,383-97,219,175 , GRCh38.p12 chr10: 92,633,626-95,459,418	CYP2C9, CYP2C19, 51 more genes
nsv3901033	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 96,522,575-96,702,831 , GRCh38.p12 chr10: 94,762,818-94,943,074	CYP2C9, CYP2C19, 5 more genes
nsv3894754	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 96,575,687-96,711,450 , GRCh38.p12 chr10: 94,815,930-94,951,693	CYP2C9, CYP2C19, 4 more genes
nsv3907664	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422	CYP2C9, SHOC2, 1487 more genes
nsv3894450	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 85,557,432-105,804,295 , GRCh38.p12 chr10: 83,797,676-104,044,537	CYP2C9, HPS1, 422 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 28

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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