Summary
Splice variantsTranscript comparisonGene allelesSequenceSecondary StructureComparative GenomicsOntologiesGO: Molecular functionGO: Biological processGO: Cellular componentPhenotypesGenetic VariationGene expressionPathwayMolecular interactionsRegulationExternal referencesSupporting evidenceID History.
C-type lectin domain family 12, member B [Source:HGNC Symbol;Acc:31966]
UNQ5782
Chromosome 12: 10,163,226-10,171,218 forward strand.
GRCh37:CM000674.1
This gene has 5 transcripts (splice variants) and 6 paralogues.
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Loading component
| Name | Chr:bp | Genomic size (bp) | Class | Source Study | Study description |
|---|---|---|---|---|---|
| nsv3904242 | 12:1-133851895 | 133851895133,851,895 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv3906484 | 12:89061-34178799 | 3408973934,089,739 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv3906723 | 12:148034-34178799 | 3403076634,030,766 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv2771722 | 12:148375-37864477 | 3771610337,716,103 | CNV | DGVa:nstd37 | Database of Genomic Variants Archive: International Standards for Cytogenetic Array Consortium |
| nsv3914427 | 12:148375-37864477 | 3771610337,716,103 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv429578 | 12:150442-11474657 | 0- | CNV | DGVa:nstd11 | Database of Genomic Variants Archive: Walter 2009 "Acquired copy number alterations in adult acute myeloid leukemia genomes." PMID:19651600 |
| nsv429630 | 12:150442-30580981 | 0- | CNV | DGVa:nstd11 | Database of Genomic Variants Archive: Walter 2009 "Acquired copy number alterations in adult acute myeloid leukemia genomes." PMID:19651600 |
| nsv984792 | 12:163819-133778796 | 133614978133,614,978 | CNV | DGVa:nstd92 | Database of Genomic Variants Archive: Forsberg 2014 "Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer." PMID:24777449 |
| nsv984743 | 12:163819-133778796 | 133614978133,614,978 | CNV | DGVa:nstd92 | Database of Genomic Variants Archive: Forsberg 2014 "Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer." PMID:24777449 |
| nsv2769822 | 12:173786-11677456 | 1150367111,503,671 | CNV | DGVa:nstd37 | Database of Genomic Variants Archive: International Standards for Cytogenetic Array Consortium |
| nsv3892478 | 12:173786-11677456 | 1150367111,503,671 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv2771391 | 12:173786-20026080 | 1985229519,852,295 | CNV | DGVa:nstd37 | Database of Genomic Variants Archive: International Standards for Cytogenetic Array Consortium |
| nsv2771897 | 12:173786-25286865 | 2511308025,113,080 | CNV | DGVa:nstd37 | Database of Genomic Variants Archive: International Standards for Cytogenetic Array Consortium |
| nsv3905613 | 12:173786-25286865 | 2511308025,113,080 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv3904488 | 12:173786-28219229 | 2804544428,045,444 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv4455458 | 12:173786-34496628 | 3432284334,322,843 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv995956 | 12:173786-34835837 | 3466205234,662,052 | CNV | DGVa:nstd37 | Database of Genomic Variants Archive: International Standards for Cytogenetic Array Consortium |
| nsv3901714 | 12:173786-34835837 | 3466205234,662,052 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv3924262 | 12:173786-34835837 | 3466205234,662,052 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv3897151 | 12:173786-37869107 | 3769532237,695,322 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv2771336 | 12:173786-37869301 | 3769551637,695,516 | CNV | DGVa:nstd37 | Database of Genomic Variants Archive: International Standards for Cytogenetic Array Consortium |
| nsv3905633 | 12:173786-37869301 | 3769551637,695,516 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv2770609 | 12:173787-133777902 | 133604116133,604,116 | CNV | DGVa:nstd37 | Database of Genomic Variants Archive: International Standards for Cytogenetic Array Consortium |
| nsv3905447 | 12:173787-133777902 | 133604116133,604,116 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
| nsv7098813 | 12:176047-34179852 | 3400380634,003,806 | CNV | dbVar:nstd102 | NCBI database of human genomic structural variation: Structural Variants with clinical assertions, submitted to ClinVar by external labs. |
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