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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5897627copy number variation1nstd209human GRCh38 chr5: 35,858,989-36,015,150 , GRCh37.p13 chr5: 35,859,091-36,015,252 UGT3A1, CAPSL-DT, 3 more genes
    nsv5842705copy number variation1nstd209human GRCh38 chr5: 35,859,001-35,868,014 , GRCh37.p13 chr5: 35,859,103-35,868,116 IL7R, LOC105374724
    nsv5673585copy number variation1nstd102humanPathogenic GRCh37 chr5: 35,857,060-35,857,181 , GRCh38.p12 chr5: 35,856,958-35,857,079 LOC105374724, IL7R
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5368153translocation1nstd200human GRCh38 chr5: 35,867,511-35,867,511 , GRCh38 chr5: 35,853,738-35,853,738 , GRCh37.p13 chr5: 35,867,613-35,867,613 , GRCh37.p13 chr5: 35,853,840-35,853,840 IL7R, LOC105374724
    nsv4937320copy number variation1nstd200human GRCh38 chr5: 35,878,289-35,878,378 , GRCh37.p13 chr5: 35,878,391-35,878,480 IL7R
    nsv4937319copy number variation1nstd200human GRCh38 chr5: 35,867,846-35,869,978 , GRCh37.p13 chr5: 35,867,948-35,870,080 IL7R
    nsv4805393copy number variation1nstd200human GRCh37 chr5: 35,859,090-36,015,254 , GRCh38.p12 chr5: 35,858,988-36,015,152 CAPSL-DT, CAPSL, 3 more genes
    nsv4802509copy number variation1nstd200human GRCh37 chr5: 35,878,391-35,878,480 , GRCh38.p12 chr5: 35,878,289-35,878,378 IL7R
    nsv4802508copy number variation1nstd200human GRCh37 chr5: 35,867,948-35,870,080 , GRCh38.p12 chr5: 35,867,846-35,869,978 IL7R
    nsv4685721copy number variation1nstd102humanPathogenic GRCh37 chr5: 35,867,357-35,867,581 , GRCh38.p12 chr5: 35,867,255-35,867,479 IL7R
    nsv4674057copy number variation1nstd102humanUncertain significance GRCh37 chr5: 35,382,352-36,123,330 , GRCh38.p12 chr5: 35,382,250-36,123,228 CAPSL, CAPSL-DT, 7 more genes
    nsv4593087copy number variation1nstd183human GRCh37 chr5: 35,858,324-35,870,117 , GRCh38.p12 chr5: 35,858,222-35,870,015 LOC105374724, IL7R
    nsv4456866copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,453,883-46,389,339 , GRCh38.p12 chr5: 34,453,778-46,389,237 LOC100506639, EEF1A1P19, 146 more genes
    nsv4450299copy number variation1nstd102humanPathogenic GRCh37 chr5: 35,860,934-35,871,335 , GRCh38 chr5: 35,860,832-35,871,233 LOC105374724, IL7R
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4412169copy number variation1nstd174human GRCh37 chr5: 35,859,079-35,873,201 , GRCh38.p12 chr5: 35,858,977-35,873,099 IL7R, LOC105374724
    nsv4344698sequence alteration1nstd166human GRCh37.p13 chr5: 35,853,813-35,867,612 , GRCh38.p12 chr5: 35,853,711-35,867,510 IL7R, LOC105374724
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