dbVar for Gene (Select 106479555) - 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
nsv5498590	copy number variation	1	nstd206	human		GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356	, RPS18P2, 713 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
nsv5004865	copy number variation	1	nstd200	human		GRCh38 chr14: 83,325,084-83,816,599 , GRCh37.p13 chr14: 83,791,428-84,282,943	RNU6ATAC28P
nsv4529423	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 83,565,970-84,403,734 , GRCh38.p12 chr14: 83,099,626-83,937,390	LINC02305, LOC107984645, 2 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	DYNLL1P2, GTF2A1, 126 more genes
nsv4226275	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 84,098,500-85,411,783 , GRCh38.p12 chr14: 83,632,156-84,945,439	LINC02305, LOC105370603, 4 more genes
nsv3923255	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr14: 83,207,988-84,427,206 , GRCh37 chr14: 84,138,235-85,357,453 , GRCh38 chr14: 83,671,891-84,891,109	LINC02305, RNU6-976P, 4 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
nsv3921857	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr14: 83,207,981-84,427,176 , GRCh38 chr14: 83,671,884-84,891,079 , GRCh37 chr14: 84,138,228-85,357,423	LINC02305, LOC105370603, 4 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
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
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	IGHV3-32, SNORD114-31, 751 more genes
nsv3912146	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr14: 78,866,819-85,421,604 , GRCh37 chr14: 79,797,066-86,351,851 , GRCh38 chr14: 79,330,723-85,885,507	DIO2, GTF2A1, 53 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
nsv3896597	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr14: 84,114,680-87,737,606 , GRCh38.p12 chr14: 83,648,336-87,271,262	LINC02305, RNU6ATAC28P, 16 more genes

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 78

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Number of Variants: 20

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