slco1b3[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
nsv3905918	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 21,086,383-21,162,243 , GRCh38.p12 chr12: 20,933,449-21,009,309	SLCO1B3-SLCO1B7
nsv6290013	insertion	2	nstd102	human	Pathogenic	GRCh38.p12 chr12: 20,861,159-20,861,159 , GRCh37 chr12: 21,014,093-21,014,093	SLCO1B3, SLCO1B3-SLCO1B7
nsv3896600	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr12: 20,968,621-21,032,468 , GRCh38.p12 chr12: 20,815,687-20,879,534	SLCO1B3, SLCO1B3-SLCO1B7
nsv3896988	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 21,017,288-21,037,895 , GRCh38.p12 chr12: 20,864,354-20,884,961	SLCO1B3, SLCO1B3-SLCO1B7
nsv3891043	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 20,996,286-21,008,004 , GRCh38.p12 chr12: 20,843,352-20,855,070	SLCO1B3, SLCO1B3-SLCO1B7
nsv3897757	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 21,196,331-21,274,334 , GRCh38.p12 chr12: 21,043,397-21,121,400	SLCO1B3-SLCO1B7, SLCO1B7
nsv3907332	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 20,998,860-21,032,242 , GRCh38.p12 chr12: 20,845,926-20,879,308	SLCO1B3, SLCO1B3-SLCO1B7
nsv4685724	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 21,017,576-21,404,166 , GRCh38.p12 chr12: 20,864,642-21,251,232	SLCO1B3, SLCO1B3-SLCO1B7, 2 more genes
nsv7137130	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 21,007,963-21,392,123 , GRCh38.p12 chr12: 20,855,029-21,239,189	SLCO1B3, SLCO1B1, 2 more genes
nsv3892484	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr12: 20,968,621-21,392,334 , GRCh38.p12 chr12: 20,815,687-21,239,400	SLCO1B3, SLCO1B7, 2 more genes
nsv3918609	copy number variation	1	nstd102	human	Benign/Likely benign	NCBI36 chr12: 20,908,843-21,247,849 , GRCh37 chr12: 21,017,576-21,356,582 , GRCh38 chr12: 20,864,642-21,203,648	SLCO1B3, SLCO1B1, 2 more genes
nsv3918226	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr12: 20,908,940-21,247,835 , GRCh37 chr12: 21,017,673-21,356,568 , GRCh38 chr12: 20,864,739-21,203,634	SLCO1B3, SLCO1B1, 2 more genes
nsv3896537	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 21,243,035-21,305,815 , GRCh38.p12 chr12: 21,090,101-21,152,881	SLCO1B1, SLCO1B7, 1 more genes
nsv3910308	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 20,876,522-21,313,256 , GRCh37.p13 chr12: 20,985,255-21,421,989 , GRCh38.p12 chr12: 20,832,321-21,269,055	SLCO1B3, SLCO1B1, 3 more genes
nsv4456617	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 21,000,817-21,415,824 , GRCh38.p12 chr12: 20,847,883-21,262,890	SLCO1B3, SLCO1B7, 3 more genes
nsv4455346	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 21,000,676-21,409,819 , GRCh38.p12 chr12: 20,847,742-21,256,885	SLCO1B3, SLCO1B1, 2 more genes
nsv4455266	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 21,007,731-21,415,824 , GRCh38.p12 chr12: 20,854,797-21,262,890	SLCO1B3, SLCO1A2, 3 more genes
nsv3900575	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 21,007,731-21,415,634 , GRCh38.p12 chr12: 20,854,797-21,262,700	SLCO1B3, SLCO1B7, 3 more genes
nsv4456475	copy number variation	3	nstd102	human	Uncertain significance	GRCh37 chr12: 21,007,731-21,415,496 , GRCh38.p12 chr12: 20,854,797-21,262,562	SLCO1B3, SLCO1B7, 2 more genes
nsv4456962	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 21,007,731-21,409,819 , GRCh38.p12 chr12: 20,854,797-21,256,885	SLCO1B3, SLCO1B3-SLCO1B7, 2 more genes

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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

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Items: 1 to 20 of 60

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Number of Variants: 20

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