arl13b[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
nsv7096967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 93,714,775-93,724,716 , GRCh38.p12 chr3: 93,995,931-94,005,872	ARL13B
nsv3874741	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 93,754,195-93,772,073 , GRCh38.p12 chr3: 94,035,351-94,053,229	ARL13B
nsv5381424	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 93,768,230-93,772,107 , GRCh38.p12 chr3: 94,049,386-94,053,263	ARL13B
nsv3870680	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 93,742,842-93,772,810 , GRCh38.p12 chr3: 94,023,998-94,053,966	ARL13B, STX19
nsv3886102	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 93,742,842-93,772,081 , GRCh38.p12 chr3: 94,023,998-94,053,237	ARL13B, STX19
nsv3874357	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 93,742,842-93,769,677 , GRCh38.p12 chr3: 94,023,998-94,050,833	ARL13B, STX19
nsv6311806	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 93,593,089-93,722,772 , GRCh38.p12 chr3: 93,874,245-94,003,928	ARL13B, PROS1, 3 more genes
nsv6314876	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 93,698,982-93,774,523 , GRCh38.p12 chr3: 93,980,138-94,055,679	ARL13B, HMGN1P7, 1 more genes
nsv7096968	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 93,772,011-93,845,334 , GRCh38.p12 chr3: 94,053,167-94,126,490	ARL13B, RBBP4P2, 2 more genes
nsv4682065	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 93,754,175-93,780,355 , GRCh38.p12 chr3: 94,035,331-94,061,511	ARL13B, DHFR2, 1 more genes
nsv7096479	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 93,692,478-93,699,346 , GRCh38.p12 chr3: 93,973,634-93,980,502	ARL13B, PROS1, 1 more genes
nsv6311807	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 93,593,089-93,845,334 , GRCh38.p12 chr3: 93,874,245-94,126,490	ARL13B, PROS1, 7 more genes
nsv3886942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 93,593,083-93,772,112 , GRCh38 chr3: 93,874,239-94,053,268	ARL13B, PROS1, 4 more genes
nsv7148201	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857	ARL13B, NECTIN3, 418 more genes
nsv3918661	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683	ARL13B, MTCO2P29, 401 more genes
nsv3917160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903	ARL13B, ATP6V1A, 297 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	ARL13B, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	ARL13B, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	ARL13B, RPL23AP49, 2875 more genes
nsv3922717	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168	ARL13B, OR7E53P, 794 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 38

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Number of Variants: 20

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Supplemental Content

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Search details

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