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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 PSTK, RNU7-12P, 1876 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 PSTK, EIF2S2P3, 895 more genes
    nsv3909943copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,213,942-135,434,178 , GRCh38 chr10: 120,454,430-133,620,674 , NCBI36 chr10: 122,203,932-135,284,168 PSTK, TEX36-AS1, 198 more genes
    nsv3892639copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,443,197-135,477,883 , GRCh38.p12 chr10: 120,683,685-133,740,558 PSTK, OR6L2P, 208 more genes
    nsv3896819copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,343,861-135,427,143 , GRCh38.p12 chr10: 120,584,349-133,613,639 PSTK, MMP21, 198 more genes
    nsv3906646copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,509,781-135,427,143 , GRCh38.p12 chr10: 120,750,269-133,613,639 PSTK, LOC105378560, 196 more genes
    nsv7098893copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,610,933-135,439,810 , GRCh38.p12 chr10: 120,851,421-133,626,306 PSTK, LOC105378571, 196 more genes
    nsv3919728copy number variation1nstd102humanPathogenic GRCh38 chr10: 120,970,558-133,622,588 , NCBI36 chr10: 122,720,061-135,286,082 , GRCh37 chr10: 122,730,071-135,436,092 PSTK, BANF1P2, 194 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 PSTK, LINC02641, 194 more genes
    nsv3909245copy number variation1nstd102humanPathogenic GRCh37 chr10: 123,019,239-135,427,143 , GRCh38.p12 chr10: 121,259,725-133,613,639 PSTK, LOC105378565, 187 more genes
    nsv3921792copy number variation1nstd102humanPathogenic NCBI36 chr10: 123,338,496-135,284,168 , GRCh37 chr10: 123,348,506-135,434,178 , GRCh38 chr10: 121,588,992-133,620,674 PSTK, LINC02641, 185 more genes
    nsv7137208copy number variation1nstd102humanPathogenic GRCh37 chr10: 123,477,898-135,427,143 , GRCh38.p12 chr10: 121,718,384-133,613,639 PSTK, ZRANB1, 182 more genes
    nsv3919634copy number variation1nstd102humanPathogenic GRCh38 chr10: 121,918,547-133,620,674 , GRCh37 chr10: 123,678,062-135,434,178 , NCBI36 chr10: 123,668,052-135,284,168 PSTK, LOC107984185, 182 more genes
    nsv1398004copy number variation1nstd102humanPathogenic GRCh37 chr10: 123,731,209-135,353,867 , GRCh38.p12 chr10: 121,971,694-133,540,363 PSTK, C10orf88B, 177 more genes
    nsv3916315copy number variation1nstd102humanPathogenic GRCh38 chr10: 122,265,252-133,620,674 , GRCh37 chr10: 124,024,767-135,434,178 , NCBI36 chr10: 124,014,757-135,284,168 PSTK, EBF3-AS1, 178 more genes
    nsv3907402copy number variation1nstd102humanPathogenic GRCh37 chr10: 124,147,428-135,370,736 , GRCh38.p12 chr10: 122,387,912-133,557,232 PSTK, BNIP3, 174 more genes
    nsv3912821copy number variation1nstd102humanPathogenic NCBI36 chr10: 124,630,713-135,284,103 , GRCh38 chr10: 122,881,207-133,620,609 , GRCh37 chr10: 124,640,723-135,434,113 PSTK, PTPRE, 164 more genes
    nsv6314129copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,019,650-125,217,066 , GRCh38.p12 chr10: 115,260,173-123,457,550 PSTK, PDZD8, 122 more genes
    nsv4349508copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,024,753-124,942,806 , GRCh38.p12 chr10: 115,265,276-123,183,290 PSTK, PRLHR, 121 more genes
    nsv3905968copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,239,239-128,203,032 , GRCh38.p12 chr10: 120,479,727-126,514,463 PSTK, MRPS21P6, 100 more genes
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