gpr156[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
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	GPR156, 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	GPR156, MTCO2P29, 401 more genes
nsv3918094	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977	GPR156, QTRT2, 284 more genes
nsv3919464	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 114,122,562-124,532,374 , GRCh37 chr3: 113,841,409-124,251,221 , NCBI36 chr3: 115,324,099-125,733,911	GPR156, B4GALT4-AS1, 144 more genes
nsv3924082	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 119,875,435-127,742,263 , GRCh38 chr3: 118,673,898-126,540,730 , GRCh37 chr3: 118,392,745-126,259,573	GPR156, MYLK-AS2, 165 more genes
nsv3919094	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 114,737,921-122,232,245 , GRCh38 chr3: 115,019,074-122,513,398 , NCBI36 chr3: 116,220,611-123,714,935	GPR156, LOC105374054, 106 more genes
nsv3923097	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 120,318,703-127,122,267 , GRCh38 chr3: 119,117,166-125,920,734 , GRCh37 chr3: 118,836,013-125,639,577	GPR156, POGLUT1, 141 more genes
nsv3875796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 115,518,341-122,129,283 , GRCh38.p12 chr3: 115,799,494-122,410,436	GPR156, SNORD155, 98 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	GPR156, 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	GPR156, 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	GPR156, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	GPR156, LINC02614, 1469 more genes
nsv6637156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502	GPR156, H1-10, 846 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	GPR156, OR7E53P, 794 more genes
nsv3880602	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 119,749,810-122,459,323 , GRCh38.p12 chr3: 120,030,963-122,740,476	GPR156, CASR, 57 more genes
nsv3880050	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 119,842,143-120,817,063 , GRCh38.p12 chr3: 120,123,296-121,098,216	GPR156, CDK2AP1P1, 20 more genes
nsv3876054	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 119,968,036-120,460,741 , GRCh38.p12 chr3: 120,249,189-120,741,894	GPR156, LOC107986121, 13 more genes
nsv6637150	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 116,109,191-120,328,013 , GRCh38.p12 chr3: 116,390,344-120,609,166	GPR156, LOC101926953, 60 more genes
nsv3917839	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 119,046,495-122,028,158 , GRCh38 chr3: 117,844,958-120,826,621 , GRCh37 chr3: 117,563,805-120,545,468	GPR156, ADPRH, 52 more genes
nsv3916767	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 117,563,805-120,515,873 , GRCh38 chr3: 117,844,958-120,797,026 , NCBI36 chr3: 119,046,495-121,998,563	GPR156, TEX55, 50 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 21

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Number of Variants: 20

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Supplemental Content

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Search details

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