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Items: 1 to 20 of 294

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952935insertion1nstd209human GRCh38 chr9: 131,430,518-131,430,518 , GRCh37.p13 chr9: 134,305,905-134,305,905 PRRC2B
    nsv5951124insertion1nstd209human GRCh38 chr9: 131,448,541-131,448,541 , GRCh37.p13 chr9: 134,323,928-134,323,928 PRRC2B
    nsv5925019copy number variation1nstd209human GRCh38 chr9: 131,454,865-131,454,952 , GRCh37.p13 chr9: 134,330,252-134,330,339 PRRC2B
    nsv5725284mobile element insertion1nstd211human GRCh38 chr9: 131,443,450-131,443,450 , GRCh37.p13 chr9: 134,318,837-134,318,837 PRRC2B
    nsv5697017mobile element insertion1nstd211human GRCh38 chr9: 131,497,862-131,497,862 , GRCh37.p13 chr9: 134,373,249-134,373,249 , PRRC2B
    nsv5637717insertion1nstd207human GRCh38 chr9: 131,430,495-131,430,495 , GRCh37.p13 chr9: 134,305,882-134,305,882 PRRC2B
    nsv5630412insertion1nstd207human GRCh38 chr9: 131,430,518-131,430,518 , GRCh37.p13 chr9: 134,305,905-134,305,905 PRRC2B
    nsv5602856copy number variation1nstd207human GRCh38 chr9: 131,454,865-131,454,952 , GRCh37.p13 chr9: 134,330,252-134,330,339 PRRC2B
    nsv5489250copy number variation1nstd206human GRCh38 chr9: 131,425,193-131,428,129 , GRCh37.p13 chr9: 134,300,580-134,303,516 PRRC2B
    nsv5487078copy number variation1nstd206human GRCh38 chr9: 131,495,253-131,495,500 , GRCh37.p13 chr9: 134,370,640-134,370,887 , PRRC2B
    nsv5486874copy number variation1nstd206human GRCh38 chr9: 131,451,126-131,451,252 , GRCh37.p13 chr9: 134,326,513-134,326,639 PRRC2B
    nsv5485448copy number variation1nstd206human GRCh38 chr9: 131,485,703-131,490,532 , GRCh37.p13 chr9: 134,361,090-134,365,919 SNORD62B, PRRC2B, 1 more genes
    nsv5397333mobile element insertion1nstd206human GRCh38 chr9: 131,497,862-131,497,913 , GRCh37.p13 chr9: 134,373,249-134,373,300 , PRRC2B
    nsv5379537translocation1nstd200human GRCh38 chr9: 131,365,326-131,365,326 , GRCh38 chr9: 131,500,133-131,500,133 , GRCh37.p13 chr9: 134,240,713-134,240,713 , GRCh37.p13 chr9: 134,375,520-134,375,520 , PRRC2B, 1 more genes
    nsv5314900copy number variation1nstd204human GRCh38.p13 chr9: 131,428,664-131,429,164 , GRCh37.p13 chr9: 134,304,051-134,304,551 PRRC2B
    nsv5309299copy number variation1nstd204human GRCh37.p13 chr9: 134,370,637-134,370,889 , GRCh38.p13 chr9: 131,495,250-131,495,502 , PRRC2B
    nsv5137329mobile element insertion1nstd203human GRCh38 chr9: 131,463,117-131,463,133 , GRCh37.p13 chr9: 134,338,504-134,338,520 PRRC2B
    nsv4843116copy number variation1nstd200human GRCh37 chr9: 134,325,879-134,330,333 , GRCh38.p12 chr9: 131,450,492-131,454,946 PRRC2B
    nsv4834893copy number variation1nstd200human GRCh37 chr9: 134,304,043-134,304,539 , GRCh38.p12 chr9: 131,428,656-131,429,152 PRRC2B
    nsv4758427insertion1nstd199human GRCh37 chr9: 134,305,883-134,305,883 , GRCh38.p12 chr9: 131,430,496-131,430,496 PRRC2B
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