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Items: 1 to 20 of 395

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972186inversion1nstd209human GRCh38 chr1: 153,884,793-153,893,590 , GRCh37.p13 chr1: 153,857,269-153,866,066 GATAD2B
    nsv5968308inversion1nstd209human GRCh38 chr1: 153,893,480-153,901,030 , GRCh37.p13 chr1: 153,865,956-153,873,506 GATAD2B
    nsv5960269insertion1nstd209human GRCh38 chr1: 153,861,796-153,861,796 , GRCh37.p13 chr1: 153,834,272-153,834,272 GATAD2B
    nsv5956426insertion1nstd209human GRCh38 chr1: 153,839,108-153,839,108 , GRCh37.p13 chr1: 153,811,584-153,811,584 GATAD2B
    nsv5952465insertion1nstd209human GRCh38 chr1: 153,876,227-153,876,227 , GRCh37.p13 chr1: 153,848,703-153,848,703 GATAD2B
    nsv5883386copy number variation1nstd209human GRCh38 chr1: 153,905,805-153,912,830 , GRCh37.p13 chr1: 153,878,281-153,885,306 GATAD2B
    nsv5880731copy number variation1nstd209human GRCh38 chr1: 153,884,861-153,885,869 , GRCh37.p13 chr1: 153,857,337-153,858,345 GATAD2B
    nsv5874560copy number variation1nstd209human GRCh38 chr1: 153,865,177-153,867,915 , GRCh37.p13 chr1: 153,837,653-153,840,391 GATAD2B
    nsv5867738copy number variation1nstd209human GRCh38 chr1: 153,879,192-153,879,326 , GRCh37.p13 chr1: 153,851,668-153,851,802 GATAD2B
    nsv5828240copy number variation1nstd209human GRCh38 chr1: 153,865,251-153,867,967 , GRCh37.p13 chr1: 153,837,727-153,840,443 GATAD2B
    nsv5828150copy number variation1nstd209human GRCh38 chr1: 153,908,909-153,912,880 , GRCh37.p13 chr1: 153,881,385-153,885,356 GATAD2B
    nsv5828149copy number variation1nstd209human GRCh38 chr1: 153,905,877-153,912,880 , GRCh37.p13 chr1: 153,878,353-153,885,356 GATAD2B
    nsv5828148copy number variation1nstd209human GRCh38 chr1: 153,884,789-153,885,888 , GRCh37.p13 chr1: 153,857,265-153,858,364 GATAD2B
    nsv5828147copy number variation1nstd209human GRCh38 chr1: 153,865,250-153,866,467 , GRCh37.p13 chr1: 153,837,726-153,838,943 GATAD2B
    nsv5724913mobile element insertion1nstd211human GRCh38 chr1: 153,842,648-153,842,648 , GRCh37.p13 chr1: 153,815,124-153,815,124 GATAD2B
    nsv5688524mobile element insertion2nstd211human GRCh38 chr1: 153,883,998-153,883,998 , GRCh37.p13 chr1: 153,856,474-153,856,474 GATAD2B
    nsv5618066insertion1nstd207human GRCh38 chr1: 153,861,795-153,861,795 , GRCh37.p13 chr1: 153,834,271-153,834,271 GATAD2B
    nsv5563991sequence alteration1nstd206human GRCh38 chr1: 153,884,801-153,893,602 , GRCh37.p13 chr1: 153,857,277-153,866,078 GATAD2B
    nsv5432781copy number variation1nstd206human GRCh38 chr1: 153,884,855-153,885,929 , GRCh37.p13 chr1: 153,857,331-153,858,405 GATAD2B
    nsv5429891copy number variation1nstd206human GRCh38 chr1: 153,910,009-153,910,542 , GRCh37.p13 chr1: 153,882,485-153,883,018 GATAD2B
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