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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6308936copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,717,600-89,720,885 , GRCh38.p12 chr10|NW_013171807.1: 173,632-176,917 , GRCh38.p12 chr10: 87,957,843-87,961,128 PTEN
    nsv5672535copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,690,793-89,693,018 , GRCh38.p12 chr10|NW_013171807.1: 146,828-149,053 , GRCh38.p12 chr10: 87,931,036-87,933,261 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|NW_013171807.1: 109,507-110,263 , GRCh38.p12 chr10: 87,893,684-87,894,440 PTEN
    nsv4682795copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,720,641-89,720,885 , GRCh38.p12 chr10|NW_013171807.1: 176,673-176,917 , GRCh38.p12 chr10: 87,960,884-87,961,128 PTEN
    nsv3885718copy number variation1nstd102humanPathogenic GRCh38 chr10: 87,960,888-87,961,124 , GRCh37.p13 chr10: 89,720,645-89,720,881 PTEN
    nsv7093898copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,717,600-89,717,786 , GRCh38.p12 chr10: 87,957,843-87,958,029 , GRCh38.p12 chr10|NW_013171807.1: 173,632-173,818 PTEN
    nsv4681175copy number variation2nstd102humanPathogenic, Likely pathogenic 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
    nsv6634516copy number variation1nstd102humanPathogenic GRCh38 chr10: 87,931,054-87,931,134 , GRCh37 chr10: 89,690,811-89,690,891 PTEN
    nsv4452623copy number variation1nstd102humanPathogenic GRCh38 chr10: 87,931,036-87,931,099 , GRCh37 chr10: 89,690,793-89,690,856 PTEN
    nsv7093120copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,692,852-89,692,905 , GRCh38 chr10: 87,933,095-87,933,148 PTEN
    nsv7093497insertion1nstd102humanPathogenic GRCh37 chr10: 89,692,936-89,692,936 , GRCh38 chr10: 87,933,179-87,933,179 PTEN
    nsv6314574insertion1nstd102humanPathogenic GRCh37 chr10: 89,692,935-89,692,935 , GRCh38 chr10: 87,933,178-87,933,178 PTEN
    nsv6290009insertion1nstd102humanPathogenic GRCh37 chr10: 89,711,945-89,711,945 , GRCh38.p12 chr10: 87,952,188-87,952,188 , GRCh38.p12 chr10|NW_013171807.1: 167,977-167,977 PTEN
    nsv5674321insertion1nstd102humanPathogenic GRCh37 chr10: 89,711,944-89,711,944 , GRCh38 chr10: 87,952,187-87,952,187 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
    nsv6309013copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 89,653,180-89,653,844 , GRCh38.p12 chr10: 87,893,423-87,894,087 , GRCh38.p12 chr10|NW_013171807.1: 109,246-109,910 PTEN
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