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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3870549copy number variation1nstd102humanPathogenic GRCh38 chr7: 156,823,109-156,829,209 , GRCh37 chr7: 156,615,803-156,621,903 LMBR1
    nsv3888101copy number variation1nstd102humanPathogenic GRCh37 chr7: 156,539,605-156,619,298 , GRCh38 chr7: 156,746,911-156,826,604 LMBR1
    nsv3876508copy number variation1nstd102humanPathogenic GRCh37 chr7: 156,570,780-156,646,750 , GRCh38 chr7: 156,778,086-156,854,056 LMBR1
    nsv3873471copy number variation1nstd102humanPathogenic GRCh37 chr7: 156,563,856-156,610,632 , GRCh38 chr7: 156,771,162-156,817,938 LMBR1
    nsv3879905copy number variation1nstd102humanPathogenic GRCh37 chr7: 156,578,108-156,594,751 , GRCh38 chr7: 156,785,414-156,802,057 LMBR1
    nsv997056copy number variation1nstd45humanPathogenic GRCh37 chr7: 156,583,796-156,584,568 , GRCh38.p12 chr7: 156,791,102-156,791,874 LMBR1
    nsv3905392copy number variation1nstd102humanBenign GRCh37 chr21: 47,609,731-47,610,939 , GRCh38.p12 chr21: 46,189,817-46,191,025 , GRCh38.p12 chr21|NT_187626.1: 51,187-52,395 LSS
    nsv7097877copy number variation1nstd102humanUncertain significance GRCh37 chr7: 156,476,772-156,629,599 , GRCh38.p12 chr7: 156,684,078-156,836,905 LMBR1
    nsv6315281copy number variation1nstd102humanPathogenic GRCh38 chr21: 46,228,666-46,229,004 , GRCh37 chr21: 47,648,580-47,648,918 LSS, MCM3AP-AS1
    nsv3907891copy number variation1nstd102humanBenign GRCh37 chr21: 47,589,136-47,610,415 , GRCh38.p12 chr21|NT_187626.1: 28,665-51,871 , GRCh38.p12 chr21: 46,169,222-46,190,501 LSS, SPATC1L
    nsv3896114copy number variation1nstd102humanBenign GRCh37 chr21: 47,589,136-47,610,305 , GRCh38.p12 chr21: 46,169,222-46,190,391 , GRCh38.p12 chr21|NT_187626.1: 28,665-51,761 LSS, SPATC1L
    nsv3891167copy number variation1nstd102humanBenign GRCh37 chr21: 47,589,156-47,610,305 , GRCh38.p12 chr21|NT_187626.1: 28,685-51,761 , GRCh38.p12 chr21: 46,169,242-46,190,391 LSS, SPATC1L
    nsv3900691copy number variation1nstd102humanBenign GRCh37 chr21: 47,589,136-47,610,085 , GRCh38.p12 chr21: 46,169,222-46,190,171 , GRCh38.p12 chr21|NT_187626.1: 28,665-51,541 LSS, SPATC1L
    nsv3896061copy number variation1nstd102humanBenign GRCh37 chr21: 47,589,277-47,610,085 , GRCh38.p12 chr21|NT_187626.1: 28,806-51,541 , GRCh38.p12 chr21: 46,169,363-46,190,171 LSS, SPATC1L
    nsv3892205copy number variation1nstd102humanBenign GRCh37 chr21: 47,589,277-47,610,066 , GRCh38.p12 chr21: 46,169,363-46,190,152 , GRCh38.p12 chr21|NT_187626.1: 28,806-51,522 LSS, SPATC1L
    nsv3908262copy number variation1nstd102humanBenign GRCh37 chr21: 47,589,429-47,610,085 , GRCh38.p12 chr21|NT_187626.1: 28,959-51,541 , GRCh38.p12 chr21: 46,169,515-46,190,171 LSS, SPATC1L
    nsv3908088copy number variation1nstd102humanBenign GRCh37 chr21: 47,589,581-47,610,085 , GRCh38.p12 chr21: 46,169,667-46,190,171 , GRCh38.p12 chr21|NT_187626.1: 31,693-51,541 LSS, SPATC1L
    nsv3899008copy number variation1nstd102humanBenign GRCh37 chr21: 47,603,387-47,610,085 , GRCh38.p12 chr21: 46,183,473-46,190,171 , GRCh38.p12 chr21|NT_187626.1: 44,843-51,541 LSS, SPATC1L
    nsv3890603copy number variation1nstd102humanBenign GRCh37 chr21: 47,603,423-47,610,085 , GRCh38.p12 chr21: 46,183,509-46,190,171 , GRCh38.p12 chr21|NT_187626.1: 44,879-51,541 LSS, SPATC1L
    nsv3908537copy number variation1nstd102humanPathogenic GRCh37 chr7: 156,460,343-156,682,575 , GRCh38.p12 chr7: 156,667,649-156,889,881 LMBR1, RNF32, 1 more genes
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