dbVar for Gene (Select 442915) - 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
nsv7148136	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,367,259-101,508,462 , GRCh38.p12 chr14: 99,900,922-101,042,125	SNORD113-5, SNORD114-27, 99 more genes
nsv6958859	copy number variation	1	nstd229	human		GRCh38 chr14: 100,868,127-101,331,726 , GRCh37.p13 chr14: 101,334,464-101,798,063	MIR136, MIR329-2, 97 more genes
nsv6637825	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229	CHGA, SNORD114-26, 676 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	PAPOLA-DT, LOC105378180, 1338 more genes
nsv6291768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 95,871,795-102,457,523 , GRCh38.p12 chr14: 95,405,458-101,991,186	CCDC85C, MEG3, 206 more genes
nsv6132885	copy number variation	1	nstd213	human		GRCh37 chr14: 99,590,000-101,630,001 , GRCh38.p12 chr14: 99,123,663-101,163,664	DLK1, MEG8, 135 more genes
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
nsv4684265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456	NDUFB3P4, LINC02320, 502 more genes
nsv4618949	copy number variation	1	nstd183	human		GRCh37 chr14: 101,372,908-101,884,282 , GRCh38.p12 chr14: 100,906,571-101,417,945	, LOC100128373, 90 more genes
nsv4456178	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229	LOC105370639, SERPINA9, 600 more genes
nsv4455156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 99,794,230-107,285,437 , GRCh38.p12 chr14: 99,327,893-106,877,229	IGHG4, IGHV3-57, 464 more genes
nsv4413532	copy number variation	1	nstd174	human		GRCh37 chr14: 101,372,741-101,967,655 , GRCh38.p12 chr14: 100,906,404-101,501,318	, MIR369, 92 more genes
nsv4349898	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 99,737,888-101,847,855 , GRCh38.p12 chr14: 99,271,551-101,381,518	EML1, WARS1, 136 more genes
nsv4349480	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,575,917-107,281,934 , GRCh38.p12 chr14: 100,109,580-106,873,725	IGHD2-21, MIR300, 452 more genes
nsv4219673	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 101,377,431-101,381,754 , GRCh38.p12 chr14: 100,911,094-100,915,417	MIR370, MEG8
nsv3924299	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,260,674-101,410,904 , GRCh38 chr14: 99,794,337-100,944,567 , NCBI36 chr14: 99,330,427-100,480,657	MIR433, RN7SKP92, 48 more genes
nsv3922827	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 100,309,382-106,855,263 , GRCh37 chr14: 100,775,719-107,263,478 , NCBI36 chr14: 99,845,472-106,334,523	RNU6-1316P, MIR136, 440 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
nsv3921506	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 99,831,655-106,855,263 , GRCh37 chr14: 100,297,992-107,263,478 , NCBI36 chr14: 99,367,745-106,334,523	RPL21P13, EXOC3L4, 453 more genes
nsv3921292	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 91,455,861-106,832,642 , GRCh37 chr14: 91,922,205-107,240,869 , NCBI36 chr14: 90,991,958-106,311,914	IGHVII-15-1, LINC03117, 594 more genes

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 97

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Number of Variants: 20

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