evc[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
nsv6312261	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,711,924-5,817,031 , GRCh38.p12 chr4: 5,710,197-5,815,304	EVC
nsv7097003	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,754,553-5,785,501 , GRCh38.p12 chr4: 5,752,826-5,783,774	EVC
nsv4681717	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,731,024-5,759,862 , GRCh38.p12 chr4: 5,729,297-5,758,135	EVC
nsv7096739	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,785,269-5,812,774 , GRCh38.p12 chr4: 5,783,542-5,811,047	EVC
nsv6312259	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,564,565-5,586,587 , GRCh38.p12 chr4: 5,562,838-5,584,860	EVC2
nsv7096735	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,564,565-5,578,191 , GRCh38.p12 chr4: 5,562,838-5,576,464	EVC2
nsv6311729	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,749,725-5,755,670 , GRCh38.p12 chr4: 5,747,998-5,753,943	EVC
nsv7097001	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,690,874-5,696,238 , GRCh38.p12 chr4: 5,689,147-5,694,511	EVC2
nsv7096864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,754,553-5,758,099 , GRCh38.p12 chr4: 5,752,826-5,756,372	EVC
nsv6311838	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,630,276-5,633,769 , GRCh38.p12 chr4: 5,628,549-5,632,042	EVC2
nsv6312263	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,803,667-5,806,578 , GRCh38.p12 chr4: 5,801,940-5,804,851	EVC
nsv4683751	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,564,575-5,567,096 , GRCh38.p12 chr4: 5,562,848-5,565,369	EVC2
nsv5673653	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,809,918-5,811,348 , GRCh38.p12 chr4: 5,808,191-5,809,621	EVC
nsv5673744	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,754,553-5,755,670 , GRCh38.p12 chr4: 5,752,826-5,753,943	EVC
nsv5673491	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,642,221-5,642,585 , GRCh38.p12 chr4: 5,640,494-5,640,858	EVC2
nsv3883739	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,798,729-5,798,979 , GRCh38 chr4: 5,797,002-5,797,252	EVC
nsv5673492	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,798,739-5,798,969 , GRCh38.p12 chr4: 5,797,012-5,797,242	EVC
nsv4683009	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,570,161-5,570,377 , GRCh38.p12 chr4: 5,568,434-5,568,650	EVC2
nsv4452232	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,690,874-5,691,080 , GRCh38 chr4: 5,689,147-5,689,353	EVC2
nsv6311922	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 5,696,052-5,696,238 , GRCh38.p12 chr4: 5,694,325-5,694,511	EVC2

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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 131

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Number of Variants: 20

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Supplemental Content

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