U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 314

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4681126copy number variation1nstd102humanPathogenic GRCh37 chr9: 127,243,637-127,267,690 , GRCh38.p12 chr9: 124,481,358-124,505,411 NR5A1
    nsv7093083copy number variation1nstd102humanPathogenic GRCh37 chr9: 127,253,202-127,253,433 , GRCh38 chr9: 124,490,923-124,491,154 NR5A1
    nsv3889405copy number variation2nstd102humanLikely pathogenic GRCh37 chr9: 127,244,699-127,245,207 , GRCh38 chr9: 124,482,420-124,482,928 NR5A1
    nsv3901974copy number variation1nstd102humanBenign GRCh37 chr20: 58,436,963-58,502,456 , GRCh38.p12 chr20: 59,861,908-59,927,401 SYCP2
    nsv3896091copy number variation1nstd102humanBenign GRCh37 chr20: 58,436,963-58,500,453 , GRCh38.p12 chr20: 59,861,908-59,925,398 SYCP2
    nsv3897518copy number variation1nstd102humanBenign GRCh37 chr20: 58,440,630-58,502,648 , GRCh38.p12 chr20: 59,865,575-59,927,593 SYCP2
    nsv3893780copy number variation1nstd102humanBenign GRCh37 chr20: 58,440,630-58,502,456 , GRCh38.p12 chr20: 59,865,575-59,927,401 SYCP2
    nsv3901614copy number variation1nstd102humanBenign GRCh37 chr20: 58,440,630-58,500,453 , GRCh38.p12 chr20: 59,865,575-59,925,398 SYCP2
    nsv3895299copy number variation1nstd102humanBenign GRCh37 chr20: 58,436,963-58,496,439 , GRCh38.p12 chr20: 59,861,908-59,921,384 SYCP2
    nsv3898474copy number variation1nstd102humanBenign GRCh37 chr20: 58,440,630-58,496,439 , GRCh38.p12 chr20: 59,865,575-59,921,384 SYCP2
    nsv4727959copy number variation1nstd197human GRCh37 chr20: 58,443,469-58,456,547 , GRCh38.p12 chr20: 59,868,414-59,881,492 SYCP2
    nsv7024998copy number variation1nstd229human GRCh38 chr20: 59,879,313-59,879,367 , GRCh37.p13 chr20: 58,454,368-58,454,422 SYCP2
    nsv6626716copy number variation32nstd224human GRCh37 chr20: 58,440,438-58,502,456 , GRCh38.p12 chr20: 59,865,383-59,927,401 SYCP2
    nsv6626823copy number variation64nstd224human GRCh37 chr20: 58,440,438-58,496,439 , GRCh38.p12 chr20: 59,865,383-59,921,384 SYCP2
    nsv6626795copy number variation4nstd224human GRCh37 chr20: 58,452,567-58,496,439 , GRCh38.p12 chr20: 59,877,512-59,921,384 SYCP2
    nsv6626715copy number variation1nstd224human GRCh37 chr20: 58,440,438-58,468,636 , GRCh38.p12 chr20: 59,865,383-59,893,581 SYCP2
    nsv6626828copy number variation4nstd224human GRCh37 chr20: 58,476,841-58,502,456 , GRCh38.p12 chr20: 59,901,786-59,927,401 SYCP2
    nsv6626796copy number variation1nstd224human GRCh37 chr20: 58,476,862-58,502,456 , GRCh38.p12 chr20: 59,901,807-59,927,401 SYCP2
    nsv6626600copy number variation3nstd224human GRCh37 chr20: 58,476,862-58,496,439 , GRCh38.p12 chr20: 59,901,807-59,921,384 SYCP2
    nsv6626586copy number variation1nstd224human GRCh37 chr20: 58,440,438-58,456,076 , GRCh38.p12 chr20: 59,865,383-59,881,021 SYCP2
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center