dbVar for Gene (Select 145200) - 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
nsv6961488	copy number variation	1	nstd229	human		GRCh38 chr14: 101,722,995-101,745,968 , GRCh37.p13 chr14: 102,189,332-102,212,305	LINC02320, LINC00239
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
nsv6314048	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 101,732,158-107,285,437 , GRCh38.p12 chr14: 101,265,821-106,877,229	IGHD4-23, XRCC3, 329 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
nsv6291499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 101,593,860-106,160,500 , GRCh38.p12 chr14: 101,127,523-105,605,042	CDC42BPB, COA8, 133 more genes
nsv6132860	copy number variation	1	nstd213	human		GRCh37 chr14: 101,940,000-102,410,001 , GRCh38.p12 chr14: 101,473,663-101,943,664	RPL26P4, DIO3, 12 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
nsv4456944	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 101,627,916-107,147,698 , GRCh38.p12 chr14: 101,161,579-106,691,681	IGHV1-58, IGHVII-60-1, 308 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
nsv4435864	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 102,161,711-102,573,503 , GRCh38.p12 chr14: 101,695,374-102,107,166	LOC107984661, RNU6-790P, 8 more genes
nsv4421870	copy number variation	1	nstd174	human		GRCh37 chr14: 102,178,179-102,199,619 , GRCh38.p12 chr14: 101,711,842-101,733,282	LINC00239, LINC02320
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
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
nsv3920123	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,729,173-102,967,034 , GRCh38 chr14: 100,262,836-102,500,697 , NCBI36 chr14: 99,798,926-102,036,787	MIR1193, SNORD114-19, 147 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 127

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Number of Variants: 20

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