dbVar for Gene (Select 140809) - 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
nsv5533226	copy number variation	1	nstd206	human		GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982	, SNORD110, 125 more genes
nsv5381806	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 67,778-974,841 , GRCh38.p12 chr20: 87,137-994,198	DEFB132, LOC101929937, 24 more genes
nsv5025044	copy number variation	1	nstd200	human		GRCh38 chr20: 580,854-703,230 , GRCh37.p13 chr20: 561,498-683,874	, TCF15, 4 more genes
nsv4865395	copy number variation	1	nstd200	human		GRCh37 chr20: 561,498-683,874 , GRCh38.p12 chr20: 580,854-703,230	, TCF15, 4 more genes
nsv4729808	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 61,568-677,437 , GRCh38.p12 chr20: 80,927-696,793	CSNK2A1, SOX12, 18 more genes
nsv4684288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-813,880 , GRCh38.p12 chr20: 82,603-833,237	DEFB129, C20orf96, 20 more genes
nsv4682672	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 389,363-746,438 , GRCh38.p12 chr20: 408,719-765,794	SCRT2, LOC107985423, 6 more genes
nsv4680506	copy number variation	1	nstd189	human		GRCh37.p13 chr20: 1-627,290 , GRCh38.p12 chr20: 79,361-646,646	, CSNK2A1, 17 more genes
nsv4676288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-1,305,971 , GRCh38.p12 chr20: 80,927-1,325,327	TBC1D20, RAD21L1, 34 more genes
nsv4676270	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-2,269,777 , GRCh38.p12 chr20: 80,927-2,289,131	LOC100289473, STK35, 60 more genes
nsv4532730	copy number variation	1	nstd166	human		GRCh37.p13 chr20: 472,998-948,000 , GRCh38.p12 chr20: 492,354-967,357	, LOC105372492, 11 more genes
nsv4457435	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 288,904-874,280 , GRCh38.p12 chr20: 308,260-893,637	LOC107985423, TCF15, 14 more genes
nsv4451753	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 157,772-706,326 , GRCh38.p12 chr20: 177,131-725,682	DEFB129, ZCCHC3, 15 more genes
nsv4349190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843	LOC105372582, LOC101929937, 473 more genes
nsv4268353	copy number variation	1	nstd166	human		GRCh37.p13 chr20: 626,830-627,746 , GRCh38.p12 chr20: 646,186-647,102	SRXN1
nsv4264181	copy number variation	1	nstd166	human		GRCh37.p13 chr20: 622,813-632,503 , GRCh38.p12 chr20: 642,169-651,859	SRXN1, LOC107985423
nsv3962959	insertion	1	nstd168	human		GRCh38 chr20: 640,888-648,446 , GRCh37.p13 chr20: 621,532-629,090	, SRXN1
nsv3924828	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr20: 519,151-607,871 , GRCh37 chr20: 571,151-659,871 , GRCh38 chr20: 590,507-679,227	LOC107985423, TCF15, 2 more genes
nsv3924759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,422,759 , GRCh38 chr20: 89,939-1,494,113 , GRCh37 chr20: 70,580-1,474,759	DEFB127, CSNK2A1, 39 more genes
nsv3923563	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,699,213 , GRCh37 chr20: 70,580-1,751,213 , GRCh38 chr20: 89,939-1,770,567	LOC101929937, DEFB132, 50 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 166

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Number of Variants: 20

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