yif1b[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
nsv3898411	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 38,752,265-38,844,709 , GRCh38.p12 chr19: 38,261,625-38,354,069	YIF1B, C19orf33, 3 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	YIF1B, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	YIF1B, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	YIF1B, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	YIF1B, BCKDHA, 1102 more genes
nsv6290300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324	YIF1B, ZNF420, 574 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	YIF1B, ZNF461, 735 more genes
nsv3912447	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688	YIF1B, MIR8077, 233 more genes
nsv3895066	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003	YIF1B, RNU6-140P, 162 more genes
nsv7095479	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147	YIF1B, HNRNPL, 45 more genes
nsv4676223	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 38,512,717-39,291,526 , GRCh38.p12 chr19: 38,022,077-38,800,886	YIF1B, MAP4K1-AS1, 25 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

yif1b[All Fields] AND 1[has_clinical] (12)
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)