slco3a1[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
nsv3893903	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 92,477,878-92,537,617 , GRCh38.p12 chr15: 91,934,648-91,994,387	SLCO3A1
nsv3890827	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 92,663,630-92,676,660 , GRCh38.p12 chr15: 92,120,400-92,133,430	SLCO3A1
nsv3908697	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 92,666,293-92,676,660 , GRCh38.p12 chr15: 92,123,063-92,133,430	SLCO3A1
nsv3897989	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 92,671,919-92,676,660 , GRCh38.p12 chr15: 92,128,689-92,133,430	SLCO3A1
nsv3900039	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 92,671,919-92,676,435 , GRCh38.p12 chr15: 92,128,689-92,133,205	SLCO3A1
nsv3905220	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 92,575,841-92,579,182 , GRCh38.p12 chr15: 92,032,611-92,035,952	SLCO3A1
nsv3909316	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 92,577,382-92,579,182 , GRCh38.p12 chr15: 92,034,152-92,035,952	SLCO3A1
nsv3924290	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 90,309,718-90,411,694 , GRCh37.p13 chr15: 92,508,714-92,610,690 , GRCh38.p12 chr15: 91,965,484-92,067,460	SLCO3A1
nsv3917456	copy number variation	1	nstd102	human	Benign	NCBI36 chr15: 90,198,224-90,393,965 , GRCh37 chr15: 92,397,220-92,592,961 , GRCh38 chr15: 91,853,990-92,049,731	SLCO3A1, LOC105370974
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	SLCO3A1, 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	SLCO3A1, 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	SLCO3A1, 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	SLCO3A1, 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	SLCO3A1, RPL31P55, 201 more genes
nsv3899918	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,197,136-102,354,857 , GRCh38.p12 chr15: 91,653,906-101,814,654	SLCO3A1, SNRPCP18, 148 more genes
nsv6112780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538	SLCO3A1, LOC105371009, 149 more genes
nsv6290316	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 88,465,861-94,411,846 , GRCh38.p12 chr15: 87,922,630-93,868,617	SLCO3A1, LOC105370964, 130 more genes
nsv3902841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 88,295,992-94,215,607 , GRCh38.p12 chr15: 87,752,761-93,672,378	SLCO3A1, BLM, 129 more genes
nsv6291795	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 89,520,451-93,926,491 , GRCh38.p12 chr15: 88,977,220-93,383,262	SLCO3A1, LINC00930, 106 more genes
nsv4456778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 91,229,877-93,677,014 , GRCh38.p12 chr15: 90,686,646-93,133,785	SLCO3A1, H2AZ2P1, 44 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 64

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Number of Variants: 20

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