ryr3[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
nsv3909555	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 34,030,192-34,071,305 , GRCh38.p12 chr15: 33,737,991-33,779,104	RYR3
nsv4729308	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr15: 33,676,561-33,707,835 , GRCh38.p12 chr15: 33,384,360-33,415,634	RYR3
nsv4674835	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 33,576,926-33,871,487 , GRCh38.p12 chr15: 33,284,725-33,579,286	RYR3, RYR3-DT
nsv3888568	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 34,034,547-34,158,266 , GRCh38 chr15: 33,742,346-33,866,065	RYR3, AVEN
nsv6309720	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 34,117,794-34,158,266 , GRCh38.p12 chr15: 33,825,593-33,866,065	RYR3, AVEN
nsv3883828	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 34,125,784-34,151,995 , GRCh38 chr15: 33,833,583-33,859,794	RYR3, AVEN
nsv4728839	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 33,583,484-33,839,194 , GRCh38.p12 chr15: 33,291,283-33,546,993	RYR3, RYR3-DT
nsv6309783	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 33,603,247-33,765,759 , GRCh38.p12 chr15: 33,311,046-33,473,558	RYR3, RYR3-DT
nsv5380761	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 34,156,329-34,156,400 , GRCh38.p12 chr15: 33,864,128-33,864,199	RYR3, AVEN
nsv3903810	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 33,481,944-33,687,915 , GRCh38.p12 chr15: 33,189,743-33,395,714	RYR3, FMN1, 3 more genes
nsv3919202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 33,469,439-33,809,641 , GRCh38 chr15: 33,177,238-33,517,440 , NCBI36 chr15: 31,256,731-31,596,933	RYR3, LOC105370759, 3 more genes
nsv4455495	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 33,428,315-33,957,759 , GRCh38.p12 chr15: 33,136,114-33,665,558	RYR3, LOC105370759, 3 more genes
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	RYR3, 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	RYR3, RNU6-18P, 1442 more genes
nsv3917652	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 20,249,886-36,169,075 , GRCh38 chr15: 23,319,714-38,089,582 , GRCh37 chr15: 22,698,522-38,381,783	RYR3, LOC105370764, 345 more genes
nsv4674936	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,421-36,861,479 , GRCh38.p12 chr15: 23,319,714-36,569,278	RYR3, SNORD115-48, 330 more genes
nsv3921026	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 22,830,109-35,283,797 , GRCh38 chr15: 25,033,869-37,204,304 , GRCh37 chr15: 25,279,016-37,496,505	RYR3, SNORD116-17, 303 more genes
nsv3915967	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 32,635,803-40,233,825 , GRCh37 chr15: 32,928,004-40,526,026 , NCBI36 chr15: 30,715,296-38,313,318	RYR3, ANP32AP1, 112 more genes
nsv3920384	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 30,405,629-37,473,561 , GRCh38 chr15: 32,326,136-39,394,068 , GRCh37 chr15: 32,618,337-39,686,269	RYR3, PGBD4, 113 more genes
nsv6315190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 33,809,650-40,027,263 , GRCh38.p12 chr15: 33,517,449-39,735,062	RYR3, RPL32P2, 84 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

Search results

Items: 1 to 20 of 55

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Number of Variants: 20

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