M2179 AND nstd157 - 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
nsv3318001	copy number variation	1	nstd157	human		GRCh37 chr12: 64,351,613-64,369,041 , GRCh38.p12 chr12: 63,957,833-63,975,261	SRGAP1
nsv3318580	copy number variation	4	nstd157	human		GRCh37 chr16: 83,196,349-83,209,154 , GRCh38.p12 chr16: 83,162,744-83,175,549	CDH13
nsv3317465	copy number variation	8	nstd157	human		GRCh37 chr16: 60,556,223-60,566,803 , GRCh38.p12 chr16: 60,522,319-60,532,899	LOC101927605
nsv3317717	copy number variation	26	nstd157	human		GRCh37 chr12: 43,021,431-43,026,485 , GRCh38.p12 chr12: 42,627,629-42,632,683	LINC02402
nsv3318905	copy number variation	1	nstd157	human		GRCh37 chr3: 118,730,933-118,821,415 , GRCh38.p12 chr3: 119,012,086-119,102,568	IGSF11
nsv3317683	copy number variation	3	nstd157	human		GRCh37 chr17: 77,365,704-77,391,145 , GRCh38.p12 chr17: 79,369,622-79,395,063	RBFOX3
nsv3318184	copy number variation	13	nstd157	human		GRCh38.p12 chr15: 97,271,952-97,287,991 , GRCh37 chr15: 97,815,182-97,831,221	LOC105371006, LINC02253
nsv3317660	copy number variation	4	nstd157	human		GRCh38.p12 chr6: 8,926,462-8,932,063 , GRCh37 chr6: 8,926,695-8,932,296	, LOC112267952
nsv3318079	copy number variation	1	nstd157	human		GRCh38.p12 chr1: 84,501,081-84,526,427 , GRCh37 chr1: 84,966,764-84,992,110	GNG5, SPATA1
nsv3317416	copy number variation	5	nstd157	human		GRCh38.p12 chr6: 32,490,391-32,553,130 , GRCh37 chr6: 32,458,168-32,520,907	HLA-DRB5, HLA-DRB6, 1 more genes
nsv3318321	copy number variation	2	nstd157	human		GRCh38.p12 chr1: 145,603,903-145,809,105 , GRCh37 chr1: 145,625,979-145,831,160	PDZK1, CD160, 3 more genes
nsv3318395	copy number variation	1	nstd157	human		GRCh37 chr5: 59,713,726-59,768,000 , GRCh38.p12 chr5: 60,417,899-60,472,173	PDE4D, RPL31P8, 1 more genes
nsv3317192	copy number variation	2	nstd157	human		GRCh37 chr2: 194,914,909-194,986,950 , GRCh38.p12 chr2: 194,050,185-194,122,226	0
nsv3318064	copy number variation	1	nstd157	human		GRCh37 chr4: 156,959,568-156,972,546 , GRCh38.p12 chr4: 156,038,416-156,051,394	0
nsv3317878	copy number variation	25	nstd157	human		GRCh37 chr3: 162,131,408-162,142,475 , GRCh38.p12 chr3: 162,413,620-162,424,687	0
nsv3317778	copy number variation	1	nstd157	human		GRCh37 chr22: 47,927,531-47,935,868 , GRCh38.p12 chr22: 47,531,782-47,540,119	0
nsv3318483	copy number variation	1	nstd157	human		GRCh37 chr7: 42,383,372-42,391,669 , GRCh38.p12 chr7: 42,343,773-42,352,070	0
nsv3318502	copy number variation	31	nstd157	human		GRCh37 chr9: 78,004,378-78,011,616 , GRCh38.p12 chr9: 75,389,462-75,396,700	0
nsv3317294	copy number variation	14	nstd157	human		GRCh38.p12 chr4: 59,114,344-59,122,377 , GRCh37 chr4: 59,980,062-59,988,095	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

M2179 AND nstd157 (20)
dbVar
Neuroblastic tumor
Neuroblastic tumor

MedGen
C1334953[conceptid] (1)
MedGen

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)