sys1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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

Search results

Items: 14

loading data ...

Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3912723	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019	SYS1, LOC107985448, 370 more genes
nsv3910049	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 33,289,165-45,693,969 , GRCh37 chr20: 33,825,749-46,260,562 , GRCh38 chr20: 35,237,946-47,631,818	SYS1, NDUFB4P10, 291 more genes
nsv6290315	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509	SYS1, PABPC1L, 170 more genes
nsv7095898	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 42,223,339-44,638,757 , GRCh38.p12 chr20: 43,594,699-46,010,118	SYS1, ADA, 99 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	SYS1, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	SYS1, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	SYS1, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	SYS1, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	SYS1, MIR3646, 1310 more genes
nsv3915005	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321	SYS1, FTLP1, 472 more genes
nsv4674805	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 34,980,430-46,806,549 , GRCh38.p12 chr20: 36,352,027-48,177,806	SYS1, ADA, 266 more genes
nsv3912203	copy number variation	1	nstd102	human	Benign	NCBI36 chr20: 43,367,016-43,436,715 , GRCh37 chr20: 43,933,602-44,003,301 , GRCh38 chr20: 45,304,962-45,374,661	SYS1, SDC4, 5 more genes
nsv3910818	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167	SYS1, RNA5SP481, 855 more genes
nsv1398401	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 43,955,980-44,053,178 , GRCh38.p12 chr20: 45,327,340-45,424,538	SYS1, SDC4, 8 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

sys1[All Fields] AND 1[has_clinical] (15)
dbVar
cytochrome b (mitochondrion) [Filchnerella helanshanensis]
cytochrome b (mitochondrion) [Filchnerella helanshanensis]
gi|452849302|ref|YP_007474971.1|

Protein
PubChem Compound Links for Gene (Select 8832) (20)
PubChem Compound
Trifolium pratense
Trifolium pratense
Trifolium pratense L. Genome sequencing and assembly

BioProject
LOC110611765 [Manihot esculenta]
LOC110611765 [Manihot esculenta]
Gene ID:110611765

Gene

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)