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Items: 1 to 20 of 308

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5942725copy number variation1nstd209human GRCh38 chr14: 95,258,993-95,259,053 , GRCh37.p13 chr14: 95,725,330-95,725,390 CLMN
    nsv5940228copy number variation1nstd209human GRCh38 chr14: 95,245,744-95,245,875 , GRCh37.p13 chr14: 95,712,081-95,712,212 CLMN
    nsv5936845copy number variation1nstd209human GRCh38 chr14: 95,245,169-95,245,264 , GRCh37.p13 chr14: 95,711,506-95,711,601 CLMN
    nsv5934453copy number variation1nstd209human GRCh38 chr14: 95,230,963-95,231,294 , GRCh37.p13 chr14: 95,697,300-95,697,631 CLMN
    nsv5853099copy number variation1nstd209human GRCh38 chr14: 95,272,573-95,274,072 , GRCh37.p13 chr14: 95,738,910-95,740,409 CLMN
    nsv5850521copy number variation1nstd209human GRCh38 chr14: 95,213,556-95,214,855 , GRCh37.p13 chr14: 95,679,893-95,681,192 CLMN
    nsv5712950mobile element insertion2nstd211human GRCh38 chr14: 95,269,967-95,269,967 , GRCh37.p13 chr14: 95,736,304-95,736,304 CLMN
    nsv5708742mobile element insertion1nstd211human GRCh38 chr14: 95,222,277-95,222,277 , GRCh37.p13 chr14: 95,688,614-95,688,614 CLMN
    nsv5700285mobile element insertion2nstd211human GRCh38 chr14: 95,282,300-95,282,300 , GRCh37.p13 chr14: 95,748,637-95,748,637 CLMN
    nsv5661013insertion1nstd207human GRCh38 chr14: 95,293,326-95,293,326 , GRCh37.p13 chr14: 95,759,663-95,759,663 CLMN
    nsv5659552insertion1nstd207human GRCh38 chr14: 95,245,208-95,245,208 , GRCh37.p13 chr14: 95,711,545-95,711,545 CLMN
    nsv5659209insertion1nstd207human GRCh38 chr14: 95,259,980-95,259,980 , GRCh37.p13 chr14: 95,726,317-95,726,317 CLMN
    nsv5655709insertion1nstd207human GRCh38 chr14: 95,319,944-95,319,944 , GRCh37.p13 chr14: 95,786,281-95,786,281 CLMN
    nsv5599536copy number variation1nstd207human GRCh38 chr14: 95,245,191-95,245,253 , GRCh37.p13 chr14: 95,711,528-95,711,590 CLMN
    nsv5509921copy number variation1nstd206human GRCh38 chr14: 95,294,605-95,303,195 , GRCh37.p13 chr14: 95,760,942-95,769,532 CLMN
    nsv5507846copy number variation1nstd206human GRCh38 chr14: 95,245,106-95,245,270 , GRCh37.p13 chr14: 95,711,443-95,711,607 CLMN
    nsv5506331copy number variation1nstd206human GRCh38 chr14: 95,240,491-95,241,408 , GRCh37.p13 chr14: 95,706,828-95,707,745 CLMN
    nsv5503149copy number variation1nstd206human GRCh38 chr14: 95,245,987-95,246,047 , GRCh37.p13 chr14: 95,712,324-95,712,384 CLMN
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5496889copy number variation1nstd206human GRCh38 chr14: 95,230,965-95,231,295 , GRCh37.p13 chr14: 95,697,302-95,697,632 CLMN
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