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Items: 1 to 20 of 813

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4350226copy number variation1nstd102humanPathogenic GRCh37 chr12: 116,622,732-116,685,976 , GRCh38.p12 chr12: 116,184,927-116,248,171 MED13L
    nsv6313930copy number variation1nstd102humanPathogenic GRCh37 chr12: 116,523,800-116,581,474 , GRCh38.p12 chr12: 116,085,995-116,143,669 MED13L
    nsv3874159copy number variation1nstd102humanPathogenic GRCh38 chr12: 115,982,183-116,022,795 , GRCh37 chr12: 116,419,988-116,460,600 MED13L
    nsv3920665copy number variation1nstd102humanPathogenic GRCh38 chr12: 116,019,418-116,054,358 , NCBI36 chr12: 114,941,606-114,976,546 , GRCh37 chr12: 116,457,223-116,492,163 MED13L
    nsv6291725copy number variation1nstd102humanPathogenic GRCh37 chr12: 116,456,529-116,488,520 , GRCh38.p12 chr12: 116,018,724-116,050,715 MED13L
    nsv7094127copy number variation1nstd102humanPathogenic GRCh37 chr12: 116,534,454-116,549,337 , GRCh38.p12 chr12: 116,096,649-116,111,532 MED13L
    nsv4684064copy number variation1nstd102humanPathogenic GRCh37 chr12: 116,534,474-116,549,317 , GRCh38.p12 chr12: 116,096,669-116,111,512 MED13L
    nsv4675385copy number variation1nstd102humanPathogenic GRCh37 chr12: 116,443,463-116,457,804 , GRCh38.p12 chr12: 116,005,658-116,019,999 MED13L
    nsv4769283copy number variation1nstd102humanPathogenic GRCh38 chr12: 116,014,142-116,019,838 , GRCh37 chr12: 116,451,947-116,457,643 MED13L
    nsv4768363copy number variation1nstd102humanPathogenic GRCh37 chr12: 116,673,140-116,676,995 , GRCh38.p12 chr12: 116,235,335-116,239,190 MED13L
    nsv7094199copy number variation1nstd102humanPathogenic GRCh37 chr12: 116,418,535-116,420,428 , GRCh38.p12 chr12: 115,980,730-115,982,623 MED13L
    nsv3896123copy number variation1nstd102humanBenign GRCh37 chr12: 116,526,507-116,536,921 , GRCh38.p12 chr12: 116,088,702-116,099,116 MED13L
    nsv3903528copy number variation1nstd102humanBenign GRCh37 chr12: 116,526,507-116,528,428 , GRCh38.p12 chr12: 116,088,702-116,090,623 MED13L
    nsv3899934copy number variation1nstd102humanBenign GRCh37 chr12: 116,526,663-116,528,428 , GRCh38.p12 chr12: 116,088,858-116,090,623 MED13L
    nsv3899261copy number variation1nstd102humanBenign GRCh37 chr12: 116,715,224-116,715,751 , GRCh38.p12 chr12: 116,277,419-116,277,946 MED13L
    nsv3895627copy number variation1nstd102humanBenign GRCh37 chr12: 116,715,268-116,715,751 , GRCh38.p12 chr12: 116,277,463-116,277,946 MED13L
    nsv3885338copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,534,454-116,534,577 , GRCh38.p12 chr12: 116,096,649-116,096,772 MED13L
    esv4005547copy number variation1estd231human GRCh37 chr12: 116,526,473-116,528,487 , GRCh38.p12 chr12: 116,088,668-116,090,682 MED13L
    nsv4456051copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,326,288-116,417,238 , GRCh38.p12 chr12: 115,888,483-115,979,433 MED13L
    nsv4455796copy number variation1nstd102humanUncertain significance GRCh37 chr12: 116,327,565-116,409,453 , GRCh38.p12 chr12: 115,889,760-115,971,648 MED13L
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