srd5a2[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
nsv3873829	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 31,524,586-31,580,971 , GRCh37.p13 chr2: 31,749,656-31,806,040	SRD5A2
nsv4347142	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 31,758,677-31,805,700 , GRCh38.p12 chr2: 31,533,607-31,580,630	SRD5A2
nsv6311666	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 31,751,266-31,758,856 , GRCh38.p12 chr2: 31,526,196-31,533,786	SRD5A2
nsv6311496	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 31,751,266-31,751,352 , GRCh38.p12 chr2: 31,526,196-31,526,282	SRD5A2
nsv3912959	delins	1	nstd102	human	Pathogenic	GRCh37 chr2: 31,757,164-31,770,106 , GRCh38 chr2: 31,532,094-31,545,036	SRD5A2
nsv7098826	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr2: 31,621,429-31,624,204 , GRCh37.p13 chr2: 31,846,498-31,849,273	SRD5A2
nsv4454359	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 31,756,421-31,756,562 , GRCh38 chr2: 31,531,351-31,531,492	SRD5A2
nsv3870883	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr2: 31,729,141-31,871,583 , GRCh38.p12 chr2: 31,504,071-31,646,514	SRD5A2
nsv3875842	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 31,729,141-31,870,697 , GRCh38.p12 chr2: 31,504,071-31,645,628	SRD5A2
nsv3887663	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr2: 31,750,429-31,805,671 , GRCh38.p12 chr2: 31,525,359-31,580,601	SRD5A2
nsv4674541	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 31,801,038-31,880,861 , GRCh38.p12 chr2: 31,575,968-31,655,792	SRD5A2
nsv4683166	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 31,751,246-31,805,989 , GRCh38.p12 chr2: 31,526,176-31,580,920	SRD5A2
nsv6290480	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr2: 31,601,811-31,868,877 , GRCh38.p12 chr2: 31,378,945-31,643,808	SRD5A2, XDH
nsv3882290	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 31,605,411-31,811,268 , GRCh38.p12 chr2: 31,382,545-31,586,199	SRD5A2, XDH
nsv4452081	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 31,601,561-31,845,670 , GRCh38.p12 chr2: 31,378,695-31,620,601	SRD5A2, XDH
nsv7096499	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr2: 31,598,226-31,805,969 , GRCh38.p12 chr2: 31,375,360-31,580,900	SRD5A2, XDH
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	SRD5A2, CYP1B1-AS1, 1649 more genes
nsv6313619	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 29,899,368-42,441,440 , GRCh38.p12 chr2: 29,676,502-42,214,300	SRD5A2, LOC107985870, 161 more genes
nsv4454991	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 29,940,473-36,813,297 , GRCh38.p12 chr2: 29,717,607-36,586,154	SRD5A2, LOC105374435, 71 more genes
nsv3885614	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 29,240,004-32,380,876 , GRCh38.p12 chr2: 29,017,138-32,155,807	SRD5A2, LOC107985861, 32 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 43

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Number of Variants: 20

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