3667899 - dbVar

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

Result Filters

loading data ...

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv515824	copy number variation	12	nstd21	human		NCBI35 chr10: 75,593,452-76,129,675 , GRCh37.p13 chr10: 75,923,446-76,459,669 , GRCh38.p12 chr10: 74,163,688-74,699,911	ADK, MRPL35P3, 6 more genes

dbGaP
Link from dbVar to dbGaP
Gene
Link from dbVar to Gene
GEO DataSets
Link from dbVar to GEO DataSets
Pathways + GO
Pathways, annotations and biological systems (BioSystems) that cite genes containing current variations.
PubMed
Link from dbVar to PubMed
Taxonomy
Link from dbVar to Taxonomy

nssv685614 (1)
dbVar
3D structures for Gene (Select 25508) (22)
Structure
Nucleotide Links for Gene (Select 25508) (44)
Nucleotide
PREDICTED: Rattus norvegicus peptidylglycine alpha-amidating monooxygenase (Pam)...
PREDICTED: Rattus norvegicus peptidylglycine alpha-amidating monooxygenase (Pam), transcript variant X1, mRNA
gi|2678969338|ref|XM_017596286.3|

Nucleotide
PREDICTED: Rattus norvegicus peptidylglycine alpha-amidating monooxygenase (Pam)...
PREDICTED: Rattus norvegicus peptidylglycine alpha-amidating monooxygenase (Pam), transcript variant X3, mRNA
gi|2678969340|ref|XM_063266683.1|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)