dbVar for Gene (Select 406986) - 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
nsv5511449	copy number variation	1	nstd206	human		GRCh38 chr14: 104,117,688-104,117,832 , GRCh37.p13 chr14: 104,584,025-104,584,169	MIR203B, MIR203A
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
nsv5005032	copy number variation	1	nstd200	human		GRCh38 chr14: 104,058,547-104,336,906 , GRCh37.p13 chr14: 104,524,884-104,803,243	ASPG, MIR203B, 4 more genes
nsv4729218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 102,615,953-107,285,437 , GRCh38.p12 chr14: 102,149,616-106,877,229	IGHV4-61, IGHD3-9, 308 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
nsv4675279	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 104,461,553-105,232,775 , GRCh38.p12 chr14: 103,995,216-104,766,438	MIR203A, ASPG, 18 more genes
nsv4624902	copy number variation	1	nstd183	human		GRCh37 chr14: 103,676,460-105,831,463 , GRCh38.p12 chr14: 103,210,123-105,365,126	, ZFYVE21, 69 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
nsv4456320	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 102,931,119-107,285,437 , GRCh38.p12 chr14: 102,464,782-106,877,229	LOC105378184, LINC02298, 302 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
nsv4424596	copy number variation	1	nstd174	human		GRCh37 chr14: 104,460,605-104,602,445 , GRCh38.p12 chr14: 103,994,268-104,136,108	TDRD9, ASPG, 4 more genes
nsv4417424	copy number variation	1	nstd174	human		GRCh37 chr14: 104,546,401-104,587,200 , GRCh38.p12 chr14: 104,080,064-104,120,863	ASPG, MIR203A, 1 more genes
nsv4350091	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 103,804,791-105,677,579 , GRCh38.p12 chr14: 103,338,454-105,211,242	AKT1, CKB, 58 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
nsv3924752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 104,251,095-107,278,770 , NCBI36 chr14: 103,320,848-106,349,815 , GRCh38 chr14: 103,784,758-106,870,558	IGHD3-10, RNU6-684P, 252 more genes
nsv3923888	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr14: 102,868,287-103,972,976 , GRCh38 chr14: 103,332,197-104,435,594 , GRCh37 chr14: 103,798,534-104,901,931	EIF5, MIR203B, 31 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

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 231

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Number of Variants: 20

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