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Items: 1 to 20 of 224

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121279copy number variation1nstd186human GRCh37 chr9: 131,199,687-131,200,305 , GRCh38.p12 chr9: 128,437,408-128,438,026 CERCAM
    nsv5925409copy number variation1nstd209human GRCh38 chr9: 128,425,002-128,425,333 , GRCh37.p13 chr9: 131,187,281-131,187,612 CERCAM
    nsv5855943copy number variation1nstd209human GRCh38 chr9: 128,419,585-128,420,856 , GRCh37.p13 chr9: 131,181,864-131,183,135 CERCAM
    nsv5590370copy number variation1nstd207human GRCh38 chr9: 128,437,814-128,437,867 , GRCh37.p13 chr9: 131,200,093-131,200,146 CERCAM
    nsv5558902sequence alteration1nstd206human GRCh38 chr9: 128,425,157-128,433,195 , GRCh37.p13 chr9: 131,187,436-131,195,474 CERCAM
    nsv5490302copy number variation1nstd206human GRCh38 chr9: 128,437,408-128,438,026 , GRCh37.p13 chr9: 131,199,687-131,200,305 CERCAM
    nsv5484536copy number variation1nstd206human GRCh38 chr9: 128,429,540-128,434,076 , GRCh37.p13 chr9: 131,191,819-131,196,355 CERCAM
    nsv5482246copy number variation1nstd206human GRCh38 chr9: 128,433,668-128,438,006 , GRCh37.p13 chr9: 131,195,947-131,200,285 CERCAM
    nsv5379526translocation1nstd200human GRCh38 chr9: 128,405,897-128,405,897 , GRCh38 chr9: 128,406,225-128,406,225 , GRCh37.p13 chr9: 131,168,504-131,168,504 , GRCh37.p13 chr9: 131,168,176-131,168,176 CERCAM
    nsv5379525translocation1nstd200human GRCh38 chr9: 128,406,221-128,406,221 , GRCh38 chr9: 128,405,589-128,405,589 , GRCh37.p13 chr9: 131,168,500-131,168,500 , GRCh37.p13 chr9: 131,167,868-131,167,868 CERCAM
    nsv5373128translocation1nstd200human GRCh38 chr9: 128,406,070-128,406,070 , GRCh38 chr9: 128,405,981-128,405,981 , GRCh37.p13 chr9: 131,168,349-131,168,349 , GRCh37.p13 chr9: 131,168,260-131,168,260 CERCAM
    nsv5334010translocation1nstd200human GRCh37 chr9: 131,168,504-131,168,504 , GRCh37 chr9: 131,168,176-131,168,176 , GRCh38.p12 chr9: 128,406,225-128,406,225 , GRCh38.p12 chr9: 128,405,897-128,405,897 CERCAM
    nsv5332899translocation1nstd200human GRCh37 chr9: 131,167,868-131,167,868 , GRCh37 chr9: 131,168,500-131,168,500 , GRCh38.p12 chr9: 128,406,221-128,406,221 , GRCh38.p12 chr9: 128,405,589-128,405,589 CERCAM
    nsv5312561copy number variation1nstd204human GRCh38.p13 chr9: 128,425,063-128,425,611 , GRCh37.p13 chr9: 131,187,342-131,187,890 CERCAM
    nsv4988390copy number variation1nstd200human GRCh38 chr9: 128,433,668-128,438,006 , GRCh37.p13 chr9: 131,195,947-131,200,285 CERCAM
    nsv4988389copy number variation1nstd200human GRCh38 chr9: 128,417,078-128,418,211 , GRCh37.p13 chr9: 131,179,357-131,180,490 CERCAM
    nsv4988388copy number variation1nstd200human GRCh38 chr9: 128,416,635-128,416,691 , GRCh37.p13 chr9: 131,178,914-131,178,970 CERCAM
    nsv4985745copy number variation1nstd200human GRCh38 chr9: 128,408,443-128,409,625 , GRCh37.p13 chr9: 131,170,722-131,171,904 CERCAM
    nsv4985740copy number variation1nstd200human GRCh38 chr9: 128,105,845-128,709,294 , GRCh37.p13 chr9: 130,868,124-131,471,573 , SET, 33 more genes
    nsv4842334copy number variation1nstd200human GRCh37 chr9: 131,195,947-131,200,285 , GRCh38.p12 chr9: 128,433,668-128,438,006 CERCAM
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