tcerg1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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

Search results

Items: 18

loading data ...

Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	TCERG1, MEGF10, 2080 more genes
nsv3884357	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440	TCERG1, TXNDC15, 962 more genes
nsv3912937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387	TCERG1, LINC01023, 783 more genes
nsv3878447	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 141,113,273-149,154,835 , GRCh38.p12 chr5: 141,733,706-149,775,272	TCERG1, LOC107986458, 111 more genes
nsv3918033	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 145,197,355-148,541,511 , NCBI36 chr5: 144,557,111-147,901,267 , GRCh37 chr5: 144,576,918-147,921,074	TCERG1, LOC100288484, 50 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	TCERG1, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	TCERG1, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	TCERG1, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	TCERG1, PJA2, 1228 more genes
nsv3878636	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,125,085-157,574,910 , GRCh38.p12 chr5: 130,789,392-158,147,902	TCERG1, LOC100288484, 551 more genes
nsv3923414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811	TCERG1, HNRNPA3P7, 514 more genes
nsv3914009	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 129,211,386-152,713,299 , GRCh38 chr5: 129,847,794-153,353,546 , GRCh37 chr5: 129,183,487-152,733,106	TCERG1, UQCRQ, 489 more genes
nsv3924856	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 140,449,756-148,890,434 , GRCh37 chr5: 140,469,572-148,910,241 , GRCh38 chr5: 141,089,988-149,530,678	TCERG1, CTB-99A3.1, 160 more genes
nsv3884275	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409	TCERG1, LOC107986368, 1258 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	TCERG1, RNU1-150P, 1757 more genes
nsv4436069	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 144,027,815-146,077,337 , GRCh38.p12 chr5: 144,648,252-146,697,774	TCERG1, GPR151, 22 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	TCERG1, LOC105378993, 2492 more genes
nsv4457090	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 140,424,333-148,985,999 , GRCh38.p12 chr5: 141,044,748-149,606,436	TCERG1, PCDHGC4, 165 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

tcerg1[All Fields] AND 1[has_clinical] (19)
dbVar
16732[HGNC] (138)
ClinVar

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)