cep128[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
nsv4728974	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr14: 81,115,750-81,213,263 , GRCh38.p12 chr14: 80,649,406-80,746,919	CEP128
nsv4455934	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 81,084,358-81,256,954 , GRCh38.p12 chr14: 80,618,014-80,790,610	CEP128
nsv3916102	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 81,094,232-81,237,941 , GRCh38 chr14: 80,627,888-80,771,597 , NCBI36 chr14: 80,163,985-80,307,694	CEP128
nsv3923418	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr14: 80,157,192-80,406,224 , GRCh37 chr14: 81,087,439-81,336,471 , GRCh38 chr14: 80,621,095-80,870,127	CEP128, HMGN2P2
nsv6313902	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 81,090,097-81,336,471 , GRCh38.p12 chr14: 80,623,753-80,870,127	CEP128, HMGN2P2
nsv6637196	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 80,523,257-80,956,658 , GRCh38.p12 chr14: 80,056,914-80,490,315	CEP128, LOC105370593, 3 more genes
nsv4455165	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 81,403,335-81,452,549 , GRCh38.p12 chr14: 80,936,991-80,986,205	CEP128, TSHR, 1 more genes
nsv4456664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 77,274,990-89,803,137 , GRCh38.p12 chr14: 76,808,647-89,336,793	CEP128, DYNLL1P2, 126 more genes
nsv3923727	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 70,028,816-82,441,728 , GRCh38 chr14: 69,562,099-81,975,384 , NCBI36 chr14: 69,098,569-81,511,481	CEP128, COX6CP11, 240 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	CEP128, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	CEP128, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	CEP128, LOC100289511, 1996 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	CEP128, DHRS7, 1946 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	CEP128, SRMP2, 1929 more genes
nsv3904265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229	CEP128, CRIP1, 1929 more genes
nsv3917422	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478	CEP128, MIR656, 1918 more genes
nsv6315524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013	CEP128, PAPOLA-DT, 1338 more genes
nsv3898512	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 73,750,741-107,285,437 , GRCh38.p12 chr14: 73,284,033-106,877,229	CEP128, MEG3, 860 more genes
nsv3922094	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 73,655,772-106,879,298 , GRCh37 chr14: 74,122,475-107,287,505 , NCBI36 chr14: 73,192,228-106,358,550	CEP128, LOC105370614, 849 more genes
nsv3915681	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 76,758,891-106,358,550 , GRCh37 chr14: 77,689,138-107,287,505 , GRCh38 chr14: 77,222,795-106,879,298	CEP128, IGHV3-32, 751 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 25

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Number of Variants: 20

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Supplemental Content

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