dbVar for Gene (Select 5720) - 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
nsv7147671	insertion	1	nstd232	human		GRCh37.p13 chr14: 24,607,009-24,607,009 , GRCh38.p12 chr14: 24,137,800-24,137,800 , GRCh38.p12 chr14\|NW_018654722.1: 438,778-438,778	PSME1, EMC9
nsv7140544	copy number variation	1	nstd232	human		GRCh37.p13 chr14: 24,607,607-24,607,680 , GRCh38.p12 chr14: 24,138,398-24,138,471 , GRCh38.p12 chr14\|NW_018654722.1: 439,376-439,449	PSME1, EMC9
nsv7139283	copy number variation	1	nstd232	human		GRCh37.p13 chr14: 24,606,412-24,606,526 , GRCh38.p12 chr14: 24,137,203-24,137,317 , GRCh38.p12 chr14\|NW_018654722.1: 438,181-438,295	PSME1, EMC9
nsv7094423	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr14: 23,242,819-25,103,366 , GRCh38.p12 chr14: 22,773,610-24,634,160	LINC00596, NGDN, 107 more genes
nsv7074310	inversion	1	nstd229	human		GRCh38 chr14: 22,076,285-27,854,954 , GRCh37.p13 chr14: 22,544,546-28,324,160	PPP1R3E, TRAJ37, 242 more genes
nsv7070619	inversion	1	nstd229	human		GRCh38 chr14: 23,713,943-24,501,695 , GRCh37.p13 chr14: 24,183,152-24,970,901	TSSK4, RIPK3, 48 more genes
nsv6941402	copy number variation	1	nstd229	human		GRCh38 chr14: 24,059,301-24,305,100 , GRCh37.p13 chr14: 24,528,510-24,774,306	PSME2, CIDEB, 27 more genes
nsv6940423	copy number variation	1	nstd229	human		GRCh38 chr14: 24,127,601-24,140,800 , GRCh37.p13 chr14: 24,596,810-24,610,009	PSME1, EMC9, 1 more genes
nsv6315513	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000	CDH24, KLHL33, 623 more genes
nsv6314715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884	HNRNPC, FOXG1, 616 more genes
nsv6143365	copy number variation	1	nstd206	human		GRCh38 chr14: 24,135,713-24,141,713 , GRCh37.p13 chr14: 24,604,922-24,610,922	PSME2, EMC9, 2 more genes
nsv6143350	copy number variation	1	nstd206	human		GRCh38 chr14: 24,105,713-24,171,713 , GRCh37.p13 chr14: 24,574,922-24,640,922	IRF9, PSME2, 9 more genes
nsv6132776	copy number variation	1	nstd213	human		GRCh37 chr14: 24,490,000-28,000,001 , GRCh38.p12 chr14: 24,020,791-27,530,795	CMA1, LTB4R, 65 more genes
nsv5263479	copy number variation	1	nstd204	human		GRCh38.p13 chr14: 24,019,501-24,275,100 , GRCh37.p13 chr14: 24,488,710-24,744,306	, RABGGTA, 26 more genes
nsv4728842	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 24,163,771-24,818,728 , GRCh38.p12 chr14: 23,694,562-24,347,428 , GRCh38.p12 chr14\|NW_018654722.1: 1-650,500	FITM1, CIDEB, 44 more genes
nsv4685750	copy number variation	1	nstd102	human	not provided	GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685	IGBP1P1, RAB2B, 579 more genes
nsv4675943	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827	TRAJ36, SEC23A-AS1, 590 more genes
nsv4349901	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,100,682-28,730,087 , GRCh38.p12 chr14: 18,324,205-28,260,881	TRAV4, UNGP2, 458 more genes
nsv4228634	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 24,598,075-24,604,140 , GRCh38.p12 chr14\|NW_018654722.1: 429,844-435,909 , GRCh38.p12 chr14: 24,128,866-24,134,931	FITM1, PSME1
nsv4225607	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 24,605,000-24,617,000 , GRCh38.p12 chr14\|NW_018654722.1: 436,769-448,769 , GRCh38.p12 chr14: 24,135,791-24,147,791	MIR7703, PSME1, 3 more genes

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Number of Variants: 20

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