79548 AND nstd173 - dbVar - NCBI

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

Search results

Items: 16

loading data ...

Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
nsv4384091	copy number variation	77	nstd173	human		GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
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
nsv4370313	copy number variation	16	nstd173	human		GRCh37 chr3: 173,239,853-173,289,640 , GRCh38.p12 chr3: 173,522,063-173,571,850	NLGN1
nsv4366601	copy number variation	9	nstd173	human		GRCh37 chr6: 104,897,819-104,929,087 , GRCh38.p12 chr6: 104,449,944-104,481,212	LOC105377918
nsv4371805	copy number variation	282	nstd173	human		GRCh37 chr11: 18,941,197-18,961,975 , GRCh38.p12 chr11: 18,919,650-18,940,428	MRGPRX1
nsv4374295	copy number variation	1	nstd173	human		GRCh37 chrX: 1,546,986-1,650,443 , GRCh38.p12 chrX: 1,428,093-1,531,550	P2RY8, ASMTL
nsv4387947	copy number variation	14	nstd173	human		GRCh37 chrX: 62,461,588-62,505,606 , GRCh38.p12 chrX: 63,241,709-63,285,729	LOC105377212, LOC100533730
nsv4366373	copy number variation	50	nstd173	human		GRCh37 chr3: 151,512,694-151,549,014 , GRCh38.p12 chr3: 151,794,906-151,831,226	AADAC, AADACL2-AS1, 1 more genes
nsv4367799	copy number variation	1	nstd173	human		GRCh37 chr12: 19,474,770-19,581,291 , GRCh38.p12 chr12: 19,321,836-19,428,357	AEBP2, PLEKHA5, 1 more genes
nsv4374860	copy number variation	1	nstd173	human		GRCh37 chr20: 43,532,388-43,571,083 , GRCh38.p12 chr20: 44,903,747-44,942,442	YWHAB, TOMM34, 1 more genes
nsv4370779	copy number variation	156	nstd173	human		GRCh37 chr5: 8,702,522-8,750,244 , GRCh38.p12 chr5: 8,702,410-8,750,132	0
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4385783	copy number variation	12	nstd173	human		GRCh37 chr14: 22,641,680-22,959,555 , GRCh38.p12 chr14: 22,173,783-22,490,567	TRDV2, TRAV41, 41 more genes
nsv4379014	copy number variation	16	nstd173	human		GRCh37 chr7: 38,295,932-38,370,792 , GRCh38.p12 chr7: 38,256,331-38,331,191	TRG, TARP, 13 more genes
nsv4374126	copy number variation	35	nstd173	human		GRCh37 chr5: 57,326,267-57,349,970 , GRCh38.p12 chr5: 58,030,440-58,054,143	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

79548 AND nstd173 (17)
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)