14-0139-004 AND nstd173 - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 19

loading data ...

Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4373371	copy number variation	21	nstd173	human		GRCh37 chr4: 134,918,953-135,191,179 , GRCh38.p12 chr4: 133,997,798-134,270,024	PABPC4L
nsv4386852	copy number variation	127	nstd173	human		GRCh37 chr8: 137,677,896-137,862,435 , GRCh38.p12 chr8: 136,665,653-136,850,192	LINC02055
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
nsv4373927	copy number variation	40	nstd173	human		GRCh37 chr2: 98,138,405-98,162,188 , GRCh38.p12 chr2: 97,521,942-97,545,725	ANKRD36B
nsv4365093	copy number variation	508	nstd173	human		GRCh37 chr13: 57,758,269-57,778,379 , GRCh38.p12 chr13: 57,184,135-57,204,245	MTCO2P3
nsv4383018	copy number variation	16	nstd173	human		GRCh37 chr3: 8,825,346-8,866,782 , GRCh38.p12 chr3: 8,783,660-8,825,097	LOC107986061
nsv4384041	copy number variation	19	nstd173	human		GRCh37 chr19: 53,525,534-53,552,228 , GRCh38.p12 chr19: 53,022,281-53,048,975	ERVV-2
nsv4387242	copy number variation	1	nstd173	human		GRCh37 chr2: 185,012,189-185,072,580 , GRCh38.p12 chr2: 184,147,462-184,207,853	LOC105373777, LOC102724340
nsv4382253	copy number variation	206	nstd173	human		GRCh37 chr12: 11,503,225-11,553,849 , GRCh38.p12 chr12: 11,350,291-11,400,915 , GRCh38.p12 chr12\|NT_187658.1: 545,254-572,349	PRB2, PRB1
nsv4386094	copy number variation	18	nstd173	human		GRCh37 chr21: 20,057,678-20,080,934 , GRCh38.p12 chr21: 18,685,360-18,708,616	MIR548XHG, MIR548X
nsv4366841	copy number variation	35	nstd173	human		GRCh37 chr1: 104,109,088-104,132,197 , GRCh38.p12 chr1: 103,566,466-103,589,575	ACTG1P4, AMY2B
nsv4369801	copy number variation	4	nstd173	human		GRCh37 chr12: 8,004,369-8,142,583 , GRCh38.p12 chr12: 7,851,773-7,989,987	SLC2A14, NANOGP1, 3 more genes
nsv4372487	copy number variation	231	nstd173	human		GRCh37 chr12: 11,219,930-11,251,705 , GRCh38.p12 chr12: 11,067,331-11,099,106	TAS2R64P, PRH1, 3 more genes
nsv4379610	copy number variation	1	nstd173	human		GRCh37 chr14: 106,328,256-107,199,805 , GRCh38.p12 chr14: 105,862,046-106,791,567 , GRCh38.p12 chr14\|NT_187600.1: 420,111-1,214,078	IGHV1-18, IGHV3-20, 167 more genes
nsv4381036	copy number variation	161	nstd173	human		GRCh37 chr16: 19,945,795-19,978,898 , GRCh38.p12 chr16: 19,934,473-19,967,576	0
nsv4370956	copy number variation	3	nstd173	human		GRCh37 chr14: 22,384,698-22,995,123 , GRCh38.p12 chr14: 21,916,523-22,526,154	TRAV14DV4, TRDD3, 96 more genes
nsv4372404	copy number variation	32	nstd173	human		GRCh37 chr7: 142,338,344-142,493,638 , GRCh38.p12 chr7: 142,630,828-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRBV27, PRSS3P2, 21 more genes
nsv4369089	copy number variation	21	nstd173	human		GRCh37 chr7: 38,286,527-38,409,689 , GRCh38.p12 chr7: 38,246,926-38,370,088	LOC103689914, TRGVA, 24 more genes
nsv4370756	copy number variation	114	nstd173	human		GRCh37 chr11: 54,701,632-54,788,759 , GRCh38.p12 chr11: 54,934,156-55,021,283	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

14-0139-004 AND nstd173 (20)
dbVar
Macrophage-enriched Sectm1a promotes efficient efferocytosis to attenuate ischem...
Macrophage-enriched Sectm1a promotes efficient efferocytosis to attenuate ischemia/reperfusion-induced cardiac injury
Macrophage-enriched Sectm1a promotes efficient efferocytosis to attenuate ischemia/reperfusion-induced cardiac injury

BioProject
3<testcok39>espsmall e, Cyrillic (1)
BioProject

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)