ccr3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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

Search results

Items: 11

loading data ...

Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3874001	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 46,243,839-46,307,968 , GRCh38.p12 chr3: 46,202,348-46,266,477	CCR3, CCR1
nsv3918161	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 46,186,825-46,352,571 , GRCh37.p13 chr3: 46,211,821-46,377,567 , GRCh38.p12 chr3: 46,170,329-46,336,076	CCR3, UQCRC2P1, 2 more genes
nsv6315166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376	CCR3, TMEM89, 129 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	CCR3, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	CCR3, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	CCR3, RPL23AP49, 2875 more genes
nsv4347762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589	CCR3, UQCRC1, 291 more genes
nsv3921797	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353	CCR3, RBM5-AS1, 185 more genes
nsv3883164	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787	CCR3, ACAA1, 344 more genes
nsv3912340	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 45,733,423-46,319,401 , GRCh38 chr3: 45,691,931-46,277,910 , NCBI36 chr3: 45,708,427-46,294,405	CCR3, LOC105377063, 14 more genes
nsv7096805	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318	CCR3, SNORA94, 120 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

ccr3[All Fields] AND 1[has_clinical] (12)
dbVar
ketoreductase [Saccharomyces cerevisiae S288C]
ketoreductase [Saccharomyces cerevisiae S288C]
gi|6319635|ref|NP_009717.1|

Protein

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)