225978 AND nstd173 - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4387213	copy number variation	434	nstd173	human		GRCh37 chr4: 34,779,032-34,824,730 , GRCh38.p12 chr4: 34,777,410-34,823,108 , GRCh38.p12 chr4\|NW_003315915.1: 269,739-315,437	LOC105378262
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4383755	copy number variation	38	nstd173	human		GRCh37 chrX: 150,695,215-150,722,241 , GRCh38.p12 chrX: 151,526,743-151,553,769	LOC105373367
nsv4372080	copy number variation	569	nstd173	human		GRCh37 chr1: 72,762,663-72,812,440 , GRCh38.p12 chr1: 72,296,980-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,982	RPL31P12, LOC105378797
nsv4378486	copy number variation	188	nstd173	human		GRCh37 chr1: 248,753,184-248,795,289 , GRCh38.p12 chr1: 248,589,883-248,631,988	OR2T10, OR2T11
nsv4371281	copy number variation	11	nstd173	human		GRCh37 chr8: 39,246,772-39,395,028 , GRCh38.p12 chr8: 39,389,253-39,537,509	ADAM5, ADAM3A
nsv4388210	copy number variation	6	nstd173	human		GRCh37 chrX: 47,875,134-47,997,394 , GRCh38.p12 chrX: 48,015,738-48,138,017	ZNF630, SPACA5B, 2 more genes
nsv4371243	copy number variation	2	nstd173	human		GRCh37 chr12: 1,944,713-1,986,237 , GRCh38.p12 chr12: 1,835,547-1,877,071 , GRCh38.p12 chr12\|NW_018654718.1: 177,691-219,215	LRTM2, LAMP1P1, 1 more genes
nsv4374985	copy number variation	188	nstd173	human		GRCh37 chr14: 73,995,761-74,024,031 , GRCh38.p12 chr14: 73,529,057-73,557,327	ACOT1, NT5CP2, 1 more genes
nsv4377031	copy number variation	3	nstd173	human		GRCh37 chr1: 1,642,090-1,670,919 , GRCh38.p12 chr1: 1,710,651-1,739,480	SLC35E2A, LOC100129381, 1 more genes
nsv4380203	copy number variation	19	nstd173	human		GRCh37 chr14: 106,890,807-106,924,839 , GRCh38.p12 chr14: 106,434,897-106,468,915 , GRCh38.p12 chr14\|NT_187600.1: 926,576-960,594	IGH, IGHVII-40-1, 4 more genes
nsv4376900	copy number variation	2	nstd173	human		GRCh37 chr9: 24,638,942-24,831,269 , GRCh38.p12 chr9: 24,638,944-24,831,271	0
nsv4387023	copy number variation	344	nstd173	human		GRCh37 chr2: 34,701,643-34,727,784 , GRCh38.p12 chr2: 34,476,576-34,502,717	0
nsv4382474	copy number variation	59	nstd173	human		GRCh37 chr17: 44,188,310-44,784,639 , GRCh38.p12 chr17: 46,110,944-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 813,043-1,226,699	RN7SL199P, ARL17A, 14 more genes
nsv4386933	copy number variation	35	nstd173	human		GRCh37 chr14: 106,530,472-106,667,115 , GRCh38.p12 chr14: 106,074,229-106,210,472 , GRCh38.p12 chr14\|NT_187600.1: 541,998-678,241	IGHV3-19, IGHV1-17, 17 more genes
nsv4378302	copy number variation	1	nstd173	human		GRCh37 chr14: 22,848,656-22,938,126 , GRCh38.p12 chr14: 22,380,253-22,469,134	TRDV2, TRDJ3, 12 more genes

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225978 AND nstd173 (17)
dbVar
Related DataSets for GEO Profiles (Select 84958797) (1)
GEO DataSets
Colorectal cancer tumors
Colorectal cancer tumors
Accession: GDS4379

GEO DataSets
Related DataSets for GEO Profiles (Select 72004703) (1)
GEO DataSets
Chronic B-lymphocytic leukemia: peripheral blood
Chronic B-lymphocytic leukemia: peripheral blood
Accession: GDS3902

GEO DataSets

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