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Items: 1 to 20 of 1054

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137670copy number variation1nstd102humannot provided GRCh38 chr2: 72,371,236-72,504,801 , GRCh37.p13 chr2: 72,598,365-72,731,930 EXOC6B
    nsv5970943inversion1nstd209human GRCh38 chr2: 72,213,368-72,214,232 , GRCh37.p13 chr2: 72,440,497-72,441,361 EXOC6B
    nsv5968088inversion1nstd209human GRCh38 chr2: 72,214,234-72,215,430 , GRCh37.p13 chr2: 72,441,363-72,442,559 EXOC6B
    nsv5967185insertion1nstd209human GRCh38 chr2: 72,508,184-72,508,184 , GRCh37.p13 chr2: 72,735,313-72,735,313 EXOC6B
    nsv5956796insertion1nstd209human GRCh38 chr2: 72,353,349-72,353,349 , GRCh37.p13 chr2: 72,580,478-72,580,478 EXOC6B
    nsv5882632copy number variation1nstd209human GRCh38 chr2: 72,288,404-72,288,480 , GRCh37.p13 chr2: 72,515,533-72,515,609 EXOC6B, RPS15AP13
    nsv5882114copy number variation1nstd209human GRCh38 chr2: 72,263,004-72,275,152 , GRCh37.p13 chr2: 72,490,133-72,502,281 EXOC6B
    nsv5878890copy number variation1nstd209human GRCh38 chr2: 72,285,342-72,288,074 , GRCh37.p13 chr2: 72,512,471-72,515,203 EXOC6B, RPS15AP13
    nsv5875445copy number variation1nstd209human GRCh38 chr2: 72,679,239-72,687,547 , GRCh37.p13 chr2: 72,906,368-72,914,676 EXOC6B
    nsv5833798copy number variation1nstd209human GRCh38 chr2: 72,679,204-72,688,021 , GRCh37.p13 chr2: 72,906,333-72,915,150 EXOC6B
    nsv5833797copy number variation2nstd209human GRCh38 chr2: 72,410,314-72,411,313 , GRCh37.p13 chr2: 72,637,443-72,638,442 EXOC6B
    nsv5833716copy number variation1nstd209human GRCh38 chr2: 72,502,003-72,505,252 , GRCh37.p13 chr2: 72,729,132-72,732,381 EXOC6B
    nsv5833715copy number variation1nstd209human GRCh38 chr2: 72,285,394-72,288,118 , GRCh37.p13 chr2: 72,512,523-72,515,247 RPS15AP13, EXOC6B
    nsv5833714copy number variation2nstd209human GRCh38 chr2: 72,267,142-72,268,395 , GRCh37.p13 chr2: 72,494,271-72,495,524 EXOC6B
    nsv5833713copy number variation1nstd209human GRCh38 chr2: 72,262,993-72,275,099 , GRCh37.p13 chr2: 72,490,122-72,502,228 EXOC6B
    nsv5833108copy number variation2nstd209human GRCh38 chr2: 72,585,739-72,587,038 , GRCh37.p13 chr2: 72,812,868-72,814,167 EXOC6B
    nsv5730406mobile element insertion1nstd211human GRCh38 chr2: 72,437,920-72,437,920 , GRCh37.p13 chr2: 72,665,049-72,665,049 EXOC6B
    nsv5729075mobile element insertion1nstd211human GRCh38 chr2: 72,308,039-72,308,039 , GRCh37.p13 chr2: 72,535,168-72,535,168 EXOC6B
    nsv5728114mobile element insertion1nstd211human GRCh38 chr2: 72,622,323-72,622,323 , GRCh37.p13 chr2: 72,849,452-72,849,452 EXOC6B
    nsv5727900mobile element insertion1nstd211human GRCh38 chr2: 72,800,852-72,800,852 , GRCh37.p13 chr2: 73,027,981-73,027,981 EXOC6B
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