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Items: 1 to 20 of 333

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6932407copy number variation1nstd229human GRCh38 chr12: 52,378,649-52,391,177 , GRCh37.p13 chr12: 52,772,433-52,784,961 KRT84
    nsv6931315copy number variation1nstd229human GRCh38 chr12: 52,372,201-52,379,000 , GRCh37.p13 chr12: 52,765,985-52,772,784 KRT84
    nsv6932894copy number variation1nstd229human GRCh38 chr12: 52,372,231-52,378,984 , GRCh37.p13 chr12: 52,766,015-52,772,768 KRT84
    nsv6928891copy number variation1nstd229human GRCh38 chr12: 52,378,354-52,383,332 , GRCh37.p13 chr12: 52,772,138-52,777,116 KRT84
    nsv6464391copy number variation1nstd223human GRCh38 chr12: 52,372,222-52,378,981 , GRCh37.p13 chr12: 52,766,006-52,772,765 KRT84
    nsv6461244copy number variation1nstd223human GRCh38 chr12: 52,375,860-52,376,307 , GRCh37.p13 chr12: 52,769,644-52,770,091 KRT84
    nsv5504777copy number variation1nstd206human GRCh38 chr12: 52,378,354-52,383,332 , GRCh37.p13 chr12: 52,772,138-52,777,116 KRT84
    nsv4972711copy number variation1nstd200human GRCh38 chr12: 52,372,222-52,378,981 , GRCh37.p13 chr12: 52,766,006-52,772,765 KRT84
    nsv4972713copy number variation1nstd200human GRCh38 chr12: 52,378,354-52,383,332 , GRCh37.p13 chr12: 52,772,138-52,777,116 KRT84
    nsv4836635copy number variation1nstd200human GRCh37 chr12: 52,772,138-52,777,116 , GRCh38.p12 chr12: 52,378,354-52,383,332 KRT84
    nsv4972712copy number variation1nstd200human GRCh38 chr12: 52,375,698-52,376,643 , GRCh37.p13 chr12: 52,769,482-52,770,427 KRT84
    nsv4843316copy number variation1nstd200human GRCh37 chr12: 52,769,482-52,770,427 , GRCh38.p12 chr12: 52,375,698-52,376,643 KRT84
    nsv4201498copy number variation1nstd166human GRCh37.p13 chr12: 52,766,006-52,772,765 , GRCh38.p12 chr12: 52,372,222-52,378,981 KRT84
    nsv3970721copy number variation1nstd168human GRCh38 chr12: 52,371,241-52,387,134 , GRCh37.p13 chr12: 52,765,025-52,780,918 KRT84
    nsv3117627copy number variation1nstd145human GRCh37 chr12: 52,777,059-52,778,139 , GRCh38.p12 chr12: 52,383,275-52,384,355 KRT84
    nsv3145008copy number variation7nstd151human GRCh37 chr12: 52,773,657-52,777,587 , GRCh38.p12 chr12: 52,379,873-52,383,803 KRT84
    nsv3150084copy number variation1nstd151human GRCh37 chr12: 52,774,144-52,777,587 , GRCh38.p12 chr12: 52,380,360-52,383,803 KRT84
    nsv3150205copy number variation13nstd151human GRCh37 chr12: 52,773,657-52,776,854 , GRCh38.p12 chr12: 52,379,873-52,383,070 KRT84
    nsv3144391copy number variation1nstd151human GRCh37 chr12: 52,774,144-52,776,854 , GRCh38.p12 chr12: 52,380,360-52,383,070 KRT84
    nsv3150722copy number variation1nstd151human GRCh37 chr12: 52,773,657-52,776,321 , GRCh38.p12 chr12: 52,379,873-52,382,537 KRT84
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