SP52381 AND nstd71 - dbVar - NCBI

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

Search results

Items: 7

loading data ...

Number of Variants: 7

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv884818	copy number variation	499	nstd71	human		NCBI36 chr6: 32,560,168-32,591,507 , GRCh37.p13 chr6: 32,452,190-32,483,529 , GRCh38.p12 chr6: 32,484,413-32,515,752	HLA-DRB5
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv873597	copy number variation	3	nstd71	human		NCBI36 chr2: 4,090,913-4,616,289 , GRCh37.p13 chr2: 4,113,038-4,638,414 , GRCh38.p12 chr2: 4,065,447-4,590,824	LOC105373397, LOC107985841, 1 more genes
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv898442	copy number variation	1	nstd71	human		NCBI36 chr11: 125,723,751-125,802,819 , GRCh37.p13 chr11: 126,218,541-126,297,609 , GRCh38.p12 chr11: 126,348,646-126,427,714	ST3GAL4, DCPS, 2 more genes
nsv913750	copy number variation	5	nstd71	human		NCBI36 chr21: 41,208,473-41,241,269 , GRCh37.p13 chr21: 42,286,603-42,319,399 , GRCh38.p12 chr21: 40,914,677-40,947,473	0
nsv884284	copy number variation	3	nstd71	human		NCBI36 chr6: 31,390,756-31,406,526 , GRCh37.p13 chr6\|NT_167246.1: 2,629,596-2,644,951 , GRCh37.p13 chr6: 31,282,777-31,298,547 , GRCh37.p13 chr6\|NT_167249.1: 2,616,487-2,632,266 , GRCh38.p12 chr6: 31,315,000-31,330,770 , GRCh38.p12 chr6\|NT_167249.2: 2,617,189-2,632,968	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

SP52381 AND nstd71 (8)
dbVar

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)