arl8b[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
nsv3905232	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 32,241-12,681,483 , GRCh37 chr3: 73,914-12,722,982 , NCBI36 chr3: 48,914-12,697,982	ARL8B, OR7E122P, 163 more genes
nsv3885461	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-12,575,409 , GRCh38.p12 chr3: 20,213-12,533,910	ARL8B, MARK2P14, 160 more genes
nsv6636276	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-11,679,509 , GRCh38.p12 chr3: 20,214-11,638,035	ARL8B, RPL23AP39, 144 more genes
nsv3906827	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 32,241-11,379,835 , GRCh37 chr3: 73,914-11,421,309 , NCBI36 chr3: 48,914-11,396,309	ARL8B, LOC107986040, 142 more genes
nsv3895550	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 20,213-11,221,602 , NCBI36 chr3: 36,891-11,238,288 , GRCh37 chr3: 61,891-11,263,288	ARL8B, SRGAP3, 141 more genes
nsv3900952	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 52,266-11,089,569 , NCBI36 chr3: 68,949-11,106,255 , GRCh37 chr3: 93,949-11,131,255	ARL8B, RPUSD3, 137 more genes
nsv3900980	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 73,914-10,672,995 , GRCh38 chr3: 32,241-10,631,310 , NCBI36 chr3: 48,914-10,647,995	ARL8B, MIR885, 131 more genes
nsv3892568	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 705,581-11,067,828 , GRCh37 chr3: 730,581-11,092,828 , GRCh38 chr3: 688,897-11,051,142	ARL8B, DUSP5P2, 126 more genes
nsv3894686	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 48,914-10,339,808 , GRCh38 chr3: 32,241-10,323,124 , GRCh37 chr3: 73,914-10,364,808	ARL8B, RPL21P17, 128 more genes
nsv4674715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-10,287,825 , GRCh38.p12 chr3: 20,213-10,246,141	ARL8B, LOC105376944, 122 more genes
nsv3889023	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-10,104,842 , GRCh38.p12 chr3: 20,213-10,063,158	ARL8B, TTLL3, 118 more genes
nsv6636296	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-9,899,605 , GRCh38.p12 chr3: 20,214-9,857,921	ARL8B, GRM7-AS1, 101 more genes
nsv6313525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-9,797,094 , GRCh38.p12 chr3: 20,213-9,755,410	ARL8B, EGOT, 95 more genes
nsv6636323	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-9,769,457 , GRCh38.p12 chr3: 20,214-9,727,773	ARL8B, LOC107984112, 92 more genes
nsv3898532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 73,914-9,616,678 , GRCh38 chr3: 32,241-9,574,994 , NCBI36 chr3: 48,914-9,591,678	ARL8B, LOC107986009, 87 more genes
nsv3900933	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 105,526-9,549,653 , NCBI36 chr3: 80,526-9,524,653 , GRCh38 chr3: 63,843-9,507,969	ARL8B, THUMPD3, 87 more genes
nsv3900360	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 32,241-9,469,506 , NCBI36 chr3: 48,914-9,486,190 , GRCh37 chr3: 73,914-9,511,190	ARL8B, LOC105376941, 86 more genes
nsv3908709	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 93,949-9,491,994 , GRCh38 chr3: 52,266-9,450,310 , NCBI36 chr3: 68,949-9,466,994	ARL8B, IL5RA, 86 more genes
nsv3906996	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 36,891-9,378,721 , GRCh37 chr3: 61,891-9,403,721 , GRCh38 chr3: 20,213-9,362,037	ARL8B, LINC01986, 85 more genes
nsv3893280	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 73,914-9,107,971 , GRCh38 chr3: 32,241-9,066,287 , NCBI36 chr3: 48,914-9,082,971	ARL8B, GRM7-AS1, 79 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 85

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Number of Variants: 20

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Search details

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