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Homo sapiens (human) genome view
Annotation Release 108 statistics   Switch to previous build

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May 2016, Annotation Release 108

This full annotation run includes the following assemblies:

Study of the human condition such as genetic and infectious disease, the intersection between genetics and the environment, and population variation is supported by a wealth of genome-scale data. These data sets include: a) numerous sequenced genomes including several which have been assembled; b) studies that examine transcript and protein existence, abundance, and differential expression; c) epigenomic and functional studies to define regulatory and other sequence elements; and d) population studies to define small and large variations in the genome, transcriptome, proteome, epigenome, or the microbiome. The result is an unprecedented amount of data and knowledge concerning human genetics that will result in breakthroughs in understanding human biology as well as significant medical advances.

A challenge facing researchers today is that of analyzing and integrating the plethora of data available. The sequence and other molecular data available provides a critical foundation for continued advances in medicine, basic research, and clinical diagnostic technologies.

The NCBI Map Viewer provides graphical displays of features on the genome assembly. Map features that can be seen along the sequence include annotated genes and transcripts, Gnomon-predicted gene and transcript models, aligned transcript and genomic sequences, RefSeq scaffolds (the 'Contig' map), the assembly tiling path (the 'Component' map), and more. For some species, additional non-sequence maps such as Genetic maps, Radiation hybrid maps, and others may be available.

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