dbVar for Gene (Select 1059) - 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
nsv5564166	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 3,190,178-3,903,961 , GRCh38.p12 chr20: 3,209,532-3,923,314	ADAM33, AP5S1, 23 more genes
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
nsv5033561	inversion	1	nstd200	human		GRCh38 chr20: 3,693,712-5,966,244 , GRCh37.p13 chr20: 3,674,359-5,946,890	, LOC107985411, 53 more genes
nsv4729952	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 3,116,478-4,199,486 , GRCh38.p12 chr20: 3,135,832-4,218,839	LOC105372508, CDC25B, 35 more genes
nsv4729947	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 3,092,739-4,939,933 , GRCh38.p12 chr20: 3,112,093-4,959,287	SF3A3P1, PRND, 46 more genes
nsv4729753	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 2,802,218-4,010,802 , GRCh38.p12 chr20: 2,821,572-4,030,155	DDRGK1, LZTS3, 40 more genes
nsv4676134	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 2,806,498-4,007,381 , GRCh38.p12 chr20: 2,825,852-4,026,734	MIR103B2, OXT, 40 more genes
nsv4457744	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 3,654,723-3,796,884 , GRCh38.p12 chr20: 3,674,076-3,816,237	ADISSP, SPEF1, 6 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
nsv4330625	inversion	1	nstd166	human		GRCh37.p13 chr20: 2,496,151-5,491,306 , GRCh38.p12 chr20: 2,515,505-5,510,660	, ADRA1D, 89 more genes
nsv3967377	copy number variation	1	nstd168	human		GRCh38 chr20: 3,760,040-3,797,652 , GRCh37.p13 chr20: 3,740,687-3,778,299	CDC25B, SPEF1, 2 more genes
nsv3923490	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 80,106-13,029,401 , NCBI36 chr20: 8,747-12,958,049 , GRCh37 chr20: 60,747-13,010,049	LINC01751, RNA5SP474, 238 more genes
nsv3922272	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 80,106-30,227,427 , NCBI36 chr20: 8,747-28,075,764 , GRCh37 chr20: 60,747-29,462,103	ISM1-AS1, CST2, 498 more genes
nsv3922038	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr20: 80,927-5,447,679 , NCBI36 chr20: 9,568-5,376,325 , GRCh37 chr20: 61,568-5,428,325	LOC105372509, SIRPD, 150 more genes
nsv3921972	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-19,074,923 , GRCh38 chr20: 89,939-19,146,279 , GRCh37 chr20: 70,580-19,126,923	PTMAP3, LOC105372517, 331 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	MIR3646, NPEPL1, 1310 more genes
nsv3919898	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-26,305,479 , GRCh38 chr20: 80,927-26,324,843 , NCBI36 chr20: 9,568-26,253,479	MIR3192, CFAP61, 473 more genes
nsv3919009	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 13,043-6,087,725 , GRCh37 chr20: 65,043-6,139,725 , GRCh38 chr20: 84,402-6,159,078	PCED1A, TBC1D20, 169 more genes
nsv3914413	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-19,000,139 , GRCh38 chr20: 89,939-19,071,495 , GRCh37 chr20: 70,580-19,052,139	ZNF343, C20orf96, 331 more genes
nsv3914070	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 80,928-18,688,031 , NCBI36 chr20: 9,569-18,616,675 , GRCh37 chr20: 61,569-18,668,675	CDC25B, LOC105372517, 324 more genes

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Items: 1 to 20 of 110

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Number of Variants: 20

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