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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4681372copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,720,641-89,725,239 , GRCh38.p12 chr10: 87,960,884-87,965,482 , GRCh38.p12 chr10|NW_013171807.1: 176,673-181,271 PTEN
    nsv3883203copy number variation1nstd102humanPathogenic GRCh38 chr10: 87,931,040-87,933,257 , GRCh37 chr10: 89,690,797-89,693,014 PTEN
    nsv4350471copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,653,441-89,654,197 , GRCh38.p12 chr10: 87,893,684-87,894,440 , GRCh38.p12 chr10|NW_013171807.1: 109,507-110,263 PTEN
    nsv4685611copy number variation1nstd102humanPathogenic GRCh38 chr10: 87,960,762-87,961,026 , GRCh37 chr10: 89,720,519-89,720,783 PTEN
    nsv4682795copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,720,641-89,720,885 , GRCh38.p12 chr10: 87,960,884-87,961,128 , GRCh38.p12 chr10|NW_013171807.1: 176,673-176,917 PTEN
    nsv3885718copy number variation1nstd102humanPathogenic GRCh38 chr10: 87,960,888-87,961,124 , GRCh37.p13 chr10: 89,720,645-89,720,881 PTEN
    nsv4681175copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,711,865-89,712,026 , GRCh38.p12 chr10: 87,952,108-87,952,269 , GRCh38.p12 chr10|NW_013171807.1: 167,897-168,058 PTEN
    nsv3889225copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,711,869-89,712,022 , GRCh38 chr10: 87,952,112-87,952,265 PTEN
    nsv3878760copy number variation1nstd102humanPathogenic GRCh38 chr10: 87,894,015-87,894,119 , GRCh37 chr10: 89,653,772-89,653,876 PTEN
    nsv3875478copy number variation1nstd102humanPathogenic GRCh38 chr10: 87,894,025-87,894,109 , GRCh37 chr10: 89,653,782-89,653,866 PTEN
    nsv4452623copy number variation1nstd102humanPathogenic GRCh38 chr10: 87,931,036-87,931,099 , GRCh37 chr10: 89,690,793-89,690,856 PTEN
    nsv4683513copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 89,711,865-89,717,786 , GRCh38.p12 chr10: 87,952,108-87,958,029 , GRCh38.p12 chr10|NW_013171807.1: 167,897-173,818 PTEN
    nsv3896516copy number variation1nstd102humanBenign GRCh37 chr10: 89,689,267-89,698,190 , GRCh38.p12 chr10: 87,929,510-87,938,433 , GRCh38.p12 chr10|NW_013171807.1: 145,302-154,225 PTEN
    nsv3892847copy number variation1nstd102humanBenign GRCh37 chr10: 89,689,282-89,698,190 , GRCh38.p12 chr10: 87,929,525-87,938,433 , GRCh38.p12 chr10|NW_013171807.1: 145,317-154,225 PTEN
    nsv3900589copy number variation1nstd102humanBenign GRCh37 chr10: 89,689,267-89,697,353 , GRCh38.p12 chr10: 87,929,510-87,937,596 , GRCh38.p12 chr10|NW_013171807.1: 145,302-153,388 PTEN
    nsv3894708copy number variation1nstd102humanBenign GRCh37 chr10: 89,689,282-89,696,588 , GRCh38.p12 chr10|NW_013171807.1: 145,317-152,623 , GRCh38.p12 chr10: 87,929,525-87,936,831 PTEN
    nsv3902314copy number variation1nstd102humanBenign GRCh37 chr10: 89,689,391-89,695,370 , GRCh38.p12 chr10|NW_013171807.1: 145,426-151,405 , GRCh38.p12 chr10: 87,929,634-87,935,613 PTEN
    nsv3905772copy number variation1nstd102humanBenign GRCh37 chr10: 89,652,878-89,657,150 , GRCh38.p12 chr10: 87,893,121-87,897,393 , GRCh38.p12 chr10|NW_013171807.1: 108,944-113,217 PTEN
    nsv3899367copy number variation1nstd102humanBenign GRCh37 chr10: 89,649,838-89,653,686 , GRCh38.p12 chr10: 87,890,081-87,893,929 , GRCh38.p12 chr10|NW_013171807.1: 105,904-109,752 PTEN
    nsv3895823copy number variation1nstd102humanBenign GRCh37 chr10: 89,652,878-89,653,686 , GRCh38.p12 chr10: 87,893,121-87,893,929 , GRCh38.p12 chr10|NW_013171807.1: 108,944-109,752 PTEN
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