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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5898580copy number variation1nstd209human GRCh38 chr3: 133,885,018-133,885,078 , GRCh37.p13 chr3: 133,603,862-133,603,922 RAB6B
    nsv5720133mobile element insertion1nstd211human GRCh38 chr3: 133,860,308-133,860,308 , GRCh37.p13 chr3: 133,579,152-133,579,152 RAB6B
    nsv5619773insertion2nstd207human GRCh38 chr3: 133,885,062-133,885,062 , GRCh37.p13 chr3: 133,603,906-133,603,906 RAB6B
    nsv5575517copy number variation1nstd207human GRCh38 chr3: 133,884,957-133,885,050 , GRCh37.p13 chr3: 133,603,801-133,603,894 RAB6B
    nsv5559372mobile element insertion1nstd206human GRCh38 chr3: 133,860,258-133,860,308 , GRCh37.p13 chr3: 133,579,102-133,579,152 RAB6B
    nsv5450174copy number variation1nstd206human GRCh38 chr3: 133,877,029-133,882,112 , GRCh37.p13 chr3: 133,595,873-133,600,956 RAB6B
    nsv5386459copy number variation1nstd186human GRCh37 chr3: 133,603,767-133,603,947 , GRCh38.p12 chr3: 133,884,923-133,885,103 RAB6B
    nsv5367047translocation1nstd200human GRCh38 chr3: 133,859,865-133,859,865 , GRCh38 chr3: 133,859,521-133,859,521 , GRCh37.p13 chr3: 133,578,709-133,578,709 , GRCh37.p13 chr3: 133,578,365-133,578,365 RAB6B
    nsv5367046translocation1nstd200human GRCh38 chr3: 133,859,260-133,859,260 , GRCh38 chr3: 133,859,888-133,859,888 , GRCh37.p13 chr3: 133,578,732-133,578,732 , GRCh37.p13 chr3: 133,578,104-133,578,104 RAB6B
    nsv5351971translocation1nstd200human GRCh38 chr3: 133,889,377-133,889,377 , GRCh38 chr3: 133,889,439-133,889,439 , GRCh37.p13 chr3: 133,608,283-133,608,283 , GRCh37.p13 chr3: 133,608,221-133,608,221 RAB6B
    nsv5343843translocation1nstd200human GRCh37 chr2: 156,528,079-156,528,079 , GRCh37 chr3: 133,609,287-133,609,287 , GRCh38.p12 chr2: 155,671,567-155,671,567 , GRCh38.p12 chr3: 133,890,443-133,890,443 RAB6B
    nsv5335420translocation1nstd200human GRCh37 chr3: 133,578,104-133,578,104 , GRCh37 chr3: 133,578,732-133,578,732 , GRCh38.p12 chr3: 133,859,888-133,859,888 , GRCh38.p12 chr3: 133,859,260-133,859,260 RAB6B
    nsv5318825copy number variation1nstd204human GRCh38.p13 chr3: 133,859,714-133,859,800 , GRCh37.p13 chr3: 133,578,558-133,578,644 RAB6B
    nsv5316556copy number variation1nstd204human GRCh38.p13 chr3: 133,885,015-133,885,524 , GRCh37.p13 chr3: 133,603,859-133,604,368 RAB6B
    nsv5172522mobile element insertion1nstd203human GRCh38 chr3: 133,890,442-133,890,457 , GRCh37.p13 chr3: 133,609,286-133,609,301 RAB6B
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4927872copy number variation1nstd200human GRCh38 chr3: 133,869,679-133,870,169 , GRCh37.p13 chr3: 133,588,523-133,589,013 RAB6B
    nsv4927871copy number variation1nstd200human GRCh38 chr3: 133,858,735-133,859,495 , GRCh37.p13 chr3: 133,577,579-133,578,339 RAB6B
    nsv4920222copy number variation1nstd200human GRCh38 chr3: 133,873,961-133,874,963 , GRCh37.p13 chr3: 133,592,805-133,593,807 RAB6B
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