MS25345 AND nstd71 - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv884034	copy number variation	17	nstd71	human		NCBI36 chr6: 30,037,034-30,045,719 , GRCh37.p13 chr6\|NT_167247.1: 1,310,918-1,319,591 , GRCh37.p13 chr6\|NT_167246.1: 1,227,649-1,236,317 , GRCh37.p13 chr6: 29,929,055-29,937,740 , GRCh38.p12 chr6: 29,961,278-29,969,963 , GRCh38.p12 chr6\|NT_167246.2: 1,222,029-1,230,697 , GRCh38.p12 chr6\|NT_167247.2: 1,305,333-1,314,006	MICD
nsv890748	copy number variation	18	nstd71	human		NCBI36 chr8: 39,350,791-39,473,097 , GRCh37.p13 chr8: 39,231,634-39,353,940 , GRCh38.p12 chr8: 39,374,115-39,496,421	ADAM3A, ADAM5
nsv879354	copy number variation	2	nstd71	human		NCBI36 chr4: 69,129,446-69,163,108 , GRCh37.p13 chr4: 69,446,851-69,480,513 , GRCh38.p12 chr4: 68,581,133-68,614,795	LOC100422402, LOC100132651
nsv893214	copy number variation	1	nstd71	human		NCBI36 chr9: 43,559,955-43,660,188 , GRCh37.p13 chr9: 43,619,959-43,720,192 , GRCh38.p12 chr9: 42,094,197-42,194,430	CNTNAP3B, LOC100420440, 2 more genes
nsv911912	copy number variation	43	nstd71	human		NCBI36 chr19: 48,060,801-48,160,500 , GRCh37.p13 chr19: 43,368,961-43,468,660 , GRCh38.p12 chr19: 42,864,809-42,964,508	CEACAMP7, PSG1, 2 more genes
nsv914684	copy number variation	27	nstd71	human		NCBI36 chr22: 23,991,725-24,113,704 , GRCh37.p13 chr22: 25,661,725-25,783,704 , GRCh38.p12 chr22: 25,265,758-25,387,737	LRP5L, IGLL3P, 2 more genes
nsv888842	copy number variation	13	nstd71	human		NCBI36 chr7: 101,900,914-102,121,342 , GRCh37.p13 chr7: 102,113,909-102,334,106 , GRCh38.p12 chr7: 102,473,462-102,693,659	UPK3BL2, SPDYE2B, 9 more genes
nsv874803	copy number variation	29	nstd71	human		NCBI36 chr2: 110,191,475-111,021,091 , GRCh37.p13 chr2: 110,834,186-111,334,482 , GRCh38.p12 chr2: 110,076,609-110,576,877	MALL, LOC107985776, 17 more genes
nsv912308	copy number variation	2	nstd71	human		NCBI36 chr19: 57,784,277-58,128,149 , GRCh37.p13 chr19: 53,092,465-53,436,337 , GRCh38.p12 chr19: 52,589,212-52,933,084	ZNF83, ZNF468, 12 more genes
nsv873477	copy number variation	11	nstd71	human		NCBI36 chr1: 246,638,776-246,862,475 , GRCh37.p13 chr1: 248,572,153-248,795,852 , GRCh38.p12 chr1: 248,408,852-248,632,551	OR2T34, OR2T2, 11 more genes
nsv890259	copy number variation	29	nstd71	human		NCBI36 chr8: 7,575,048-7,781,955 , GRCh37.p13 chr8: 7,537,638-7,744,545 , GRCh38.p12 chr8\|NW_018654717.1: 5,303,324-5,484,311 , GRCh38.p12 chr8: 7,680,116-7,887,023	PRR23D3P, , 35 more genes

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MS25345 AND nstd71 (13)
dbVar
MS22678 AND nstd71 (11)
dbVar
Atherosclerotic left anterior descendent coronary artery: high scan
Atherosclerotic left anterior descendent coronary artery: high scan
Accession: GDS3698

GEO DataSets
Related DataSets for GEO Profiles (Select 65174409) (1)
GEO DataSets
MAG: Segatella bryantii isolate SRR11861928_bin.48_metaWRAP_v1.3_MAG ERZ14209125...
MAG: Segatella bryantii isolate SRR11861928_bin.48_metaWRAP_v1.3_MAG ERZ14209125.9224, whole genome shotgun sequence
gi|2486444258|ref|NZ_CAMUXW01000006 gnl|WGS:NZ_CAMUXW01|ERZ14209125.9224

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