dbVar for Gene (Select 2353) - 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
nsv5980451	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321	ACTN1, ACYP1, 400 more genes
nsv5032025	inversion	1	nstd200	human		GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221	, IFT43, 578 more genes
nsv4630226	copy number variation	1	nstd183	human		GRCh37 chr14: 75,740,542-75,763,164 , GRCh38.p12 chr14: 75,273,839-75,296,461	FOS, DPPA5P4, 1 more genes
nsv4372472	copy number variation	1	nstd173	human		GRCh37 chr14: 75,643,603-75,755,680 , GRCh38.p12 chr14: 75,176,900-75,288,977	TMED10, RNU4ATAC14P, 1 more genes
nsv4349747	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 74,040,231-76,368,547 , GRCh38.p12 chr14: 73,573,527-75,902,204	ACYP1, ENTPD5, 72 more genes
nsv4220896	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 75,738,000-75,747,000 , GRCh38.p12 chr14: 75,271,297-75,280,297	FOS
nsv3924066	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 75,452,898-76,865,601 , GRCh38 chr14: 74,986,195-76,399,258 , NCBI36 chr14: 74,522,651-75,935,354	RPS24P2, EIF2B2, 29 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
nsv3923448	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 73,413,528-77,578,518 , GRCh38 chr14: 73,877,072-78,042,422 , GRCh37 chr14: 74,343,775-78,508,765	ZC2HC1C, RPL21P10, 113 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	LOC105370614, LOC105370617, 849 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	SRMP2, IGHV3-71, 1929 more genes
nsv3919051	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr14: 72,879,674-78,371,155 , GRCh37 chr14: 73,809,921-79,301,402 , GRCh38 chr14: 73,343,213-78,835,059	ACYP1, ENTPD5, 137 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	MIR656, TRAJ59, 1918 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	BANF1P1, IGHV1-68, 1996 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	CRIP1, GPATCH2L, 1929 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	DHRS7, MIR548Y, 1946 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	LOC440181, HEATR5A-DT, 1998 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	LOC100289511, RNU6-552P, 1996 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	MEG3, IGHV7-27, 860 more genes
nsv3168616	copy number variation	1	nstd158	human		GRCh38.p12 chr14: 63,156,948-86,570,963 , GRCh37 chr14: 63,623,666-87,037,307	, ACTN1, 394 more genes

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Number of Variants: 20

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