ccser1[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
nsv3879505	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 91,797,748-92,473,294 , GRCh38.p12 chr4: 90,876,597-91,552,143	CCSER1
nsv3882857	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 91,406,782-91,667,562 , GRCh38.p12 chr4: 90,485,631-90,746,411	CCSER1
nsv3882091	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,271,678-92,286,445 , GRCh38.p12 chr4: 91,350,527-91,365,294	CCSER1
nsv3874169	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 91,927,272-91,941,868 , GRCh38.p12 chr4: 91,006,121-91,020,717	CCSER1
nsv3881882	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 91,886,501-91,900,701 , GRCh38.p12 chr4: 90,965,350-90,979,550	CCSER1
nsv3873731	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 91,926,462-91,933,628 , GRCh38.p12 chr4: 91,005,311-91,012,477	CCSER1
nsv3887414	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,280,933-92,286,553 , GRCh38.p12 chr4: 91,359,782-91,365,402	CCSER1
nsv3884655	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,466,958-92,761,582 , GRCh38.p12 chr4: 91,545,807-91,840,431	CCSER1
nsv3889955	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 91,934,500-92,200,866 , GRCh38.p12 chr4: 91,013,349-91,279,715	CCSER1
nsv3887059	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 91,934,500-92,185,714 , GRCh38.p12 chr4: 91,013,349-91,264,563	CCSER1
nsv3874030	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,352,498-92,477,566 , GRCh38.p12 chr4: 91,431,347-91,556,415	CCSER1
nsv3877450	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,154,401-92,258,471 , GRCh38.p12 chr4: 91,233,250-91,337,320	CCSER1
nsv3879242	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,185,714-92,258,471 , GRCh38.p12 chr4: 91,264,563-91,337,320	CCSER1
nsv3872907	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,151,187-92,185,714 , GRCh38.p12 chr4: 91,230,036-91,264,563	CCSER1
nsv3885568	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,151,187-92,183,151 , GRCh38.p12 chr4: 91,230,036-91,262,000	CCSER1
nsv3878125	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,151,187-92,179,229 , GRCh38.p12 chr4: 91,230,036-91,258,078	CCSER1
nsv3888362	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,151,187-92,172,833 , GRCh38.p12 chr4: 91,230,036-91,251,682	CCSER1
nsv3880286	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,142,966-92,163,756 , GRCh38.p12 chr4: 91,221,815-91,242,605	CCSER1
nsv3884762	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,154,401-92,172,833 , GRCh38.p12 chr4: 91,233,250-91,251,682	CCSER1
nsv3871444	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 92,151,187-92,163,756 , GRCh38.p12 chr4: 91,230,036-91,242,605	CCSER1

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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 75

Page of 4

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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