cacna1b[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
nsv7097940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 140,846,706-140,851,299 , GRCh38.p12 chr9: 137,952,254-137,956,847	CACNA1B
nsv7097939	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 140,807,612-140,811,903 , GRCh38.p12 chr9: 137,913,160-137,917,451	CACNA1B
nsv7098443	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 140,919,387-140,919,644 , GRCh38.p12 chr9: 138,024,935-138,025,192	CACNA1B
nsv7098073	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 140,972,546-141,000,279 , GRCh38.p12 chr9: 138,078,094-138,105,827	CACNA1B
nsv3890980	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 140,866,826-140,928,675 , GRCh38.p12 chr9: 137,972,374-138,034,223	CACNA1B
nsv3894906	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 140,866,689-140,915,980 , GRCh38.p12 chr9: 137,972,237-138,021,528	CACNA1B
nsv3892462	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 140,912,517-140,928,675 , GRCh38.p12 chr9: 138,018,065-138,034,223	CACNA1B
nsv3908331	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 140,912,517-140,913,833 , GRCh38.p12 chr9: 138,018,065-138,019,381	CACNA1B
nsv7097942	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 140,990,916-141,016,451 , GRCh38.p12 chr9: 138,096,464-138,121,999	CACNA1B
nsv7098074	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 141,000,131-141,016,451 , GRCh38.p12 chr9: 138,105,679-138,121,999	CACNA1B
nsv7097710	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 141,000,131-141,013,240 , GRCh38.p12 chr9: 138,105,679-138,118,788	CACNA1B
nsv7097711	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 141,008,810-141,016,451 , GRCh38.p12 chr9: 138,114,358-138,121,999	CACNA1B
nsv7097943	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 141,014,597-141,016,451 , GRCh38.p12 chr9: 138,120,145-138,121,999	CACNA1B
nsv5564527	insertion	6	nstd102	human	Uncertain significance, Likely pathogenic	GRCh38 chr9: 137,879,160-137,879,160 , GRCh37 chr9: 140,773,612-140,773,612	CACNA1B, LOC100133077
nsv3890199	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr9: 140,862,504-140,994,780 , GRCh38.p12 chr9: 137,968,052-138,100,328	CACNA1B, LOC101928786
nsv4455474	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 140,920,430-141,020,389 , GRCh38.p12 chr9: 138,025,978-138,125,937	CACNA1B, LOC101928786
nsv4455284	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 140,859,469-141,020,389 , GRCh38.p12 chr9: 137,965,017-138,125,937	CACNA1B, LOC101928786
nsv4457245	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 140,906,174-141,020,389 , GRCh38.p12 chr9: 138,011,722-138,125,937	CACNA1B, LOC101928786
nsv7097709	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 140,907,561-141,016,451 , GRCh38.p12 chr9: 138,013,109-138,121,999	CACNA1B, LOC101928786
nsv7097941	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 140,917,443-141,016,451 , GRCh38.p12 chr9: 138,022,991-138,121,999	CACNA1B, LOC101928786

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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 124

Page of 7

Number of Variants: 20

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