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Items: 1 to 20 of 36909

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3875958copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 81,367,334-81,410,823 , GRCh38 chr16: 81,333,729-81,377,218 GAN
    nsv6309883copy number variation1nstd102humanUncertain significance GRCh37 chr16: 81,348,719-81,411,201 , GRCh38.p12 chr16: 81,315,114-81,377,596 GAN
    nsv7095102copy number variation1nstd102humanUncertain significance GRCh37 chr16: 81,348,719-81,396,236 , GRCh38.p12 chr16: 81,315,114-81,362,631 GAN
    nsv6310019copy number variation1nstd102humanUncertain significance GRCh37 chr16: 81,396,084-81,411,201 , GRCh38.p12 chr16: 81,362,479-81,377,596 GAN
    nsv7095048copy number variation1nstd102humanUncertain significance GRCh37 chr16: 81,348,719-81,348,905 , GRCh38.p12 chr16: 81,315,114-81,315,300 GAN
    nsv6988787copy number variation1nstd229human GRCh38 chr16: 81,335,436-81,345,992 , GRCh37.p13 chr16: 81,369,041-81,379,597 GAN
    nsv6989650copy number variation1nstd229human GRCh38 chr16: 81,368,538-81,377,855 , GRCh37.p13 chr16: 81,402,143-81,411,460 GAN
    nsv6995252copy number variation1nstd229human GRCh38 chr16: 81,386,316-81,394,317 , GRCh37.p13 chr16: 81,419,921-81,427,922 GAN
    nsv6991976copy number variation1nstd229human GRCh38 chr16: 81,324,985-81,328,948 , GRCh37.p13 chr16: 81,358,590-81,362,553 GAN
    nsv6996423copy number variation1nstd229human GRCh38 chr16: 81,338,537-81,340,720 , GRCh37.p13 chr16: 81,372,142-81,374,325 GAN
    nsv6989869copy number variation1nstd229human GRCh38 chr16: 81,327,616-81,327,644 , GRCh37.p13 chr16: 81,361,221-81,361,249 GAN
    nsv6506044copy number variation1nstd223human GRCh38 chr16: 81,386,316-81,394,315 , GRCh37.p13 chr16: 81,419,921-81,427,920 GAN
    nsv6505918copy number variation1nstd223human GRCh38 chr16: 81,339,267-81,339,882 , GRCh37.p13 chr16: 81,372,872-81,373,487 GAN
    nsv6497262copy number variation1nstd223human GRCh38 chr16: 81,332,195-81,332,760 , GRCh37.p13 chr16: 81,365,800-81,366,365 GAN
    nsv6497136copy number variation1nstd223human GRCh38 chr16: 81,386,294-81,386,845 , GRCh37.p13 chr16: 81,419,899-81,420,450 GAN
    nsv6509698copy number variation1nstd223human GRCh38 chr16: 81,368,207-81,368,715 , GRCh37.p13 chr16: 81,401,812-81,402,320 GAN
    nsv5009681copy number variation1nstd200human GRCh38 chr16: 81,368,671-81,369,742 , GRCh37.p13 chr16: 81,402,276-81,403,347 GAN
    nsv5009679copy number variation1nstd200human GRCh38 chr16: 81,332,083-81,333,125 , GRCh37.p13 chr16: 81,365,688-81,366,730 GAN
    nsv4866892copy number variation1nstd200human GRCh37 chr16: 81,365,688-81,366,730 , GRCh38.p12 chr16: 81,332,083-81,333,125 GAN
    nsv5009680copy number variation1nstd200human GRCh38 chr16: 81,366,994-81,367,163 , GRCh37.p13 chr16: 81,400,599-81,400,768 GAN
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