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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5922602copy number variation1nstd209human GRCh38 chr10: 132,736,003-132,813,784 , GRCh37.p13 chr10: 134,549,507-134,627,288 CFAP46, INPP5A, 1 more genes
    nsv5865756copy number variation1nstd209human GRCh38 chr10: 132,775,346-132,782,454 , GRCh37.p13 chr10: 134,588,850-134,595,958 NKX6-2, INPP5A
    nsv5672526copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,548,166-135,440,251 , GRCh38.p12 chr10: 125,859,597-133,626,747 LINC00601, RPL5P28, 110 more genes
    nsv5381769copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,483,682-135,434,178 , GRCh38.p12 chr10: 127,685,418-133,620,674 DPYSL4, LINC02667, 88 more genes
    nsv5354624translocation1nstd200human GRCh38 chr10: 132,784,177-132,784,177 , GRCh38 chr10: 132,784,098-132,784,098 , GRCh37.p13 chr10: 134,597,681-134,597,681 , GRCh37.p13 chr10: 134,597,602-134,597,602 NKX6-2
    nsv4984047copy number variation1nstd200human GRCh38 chr10: 132,752,541-132,948,682 , GRCh37.p13 chr10: 134,566,045-134,762,186 CFAP46, LINC01166, 4 more genes
    nsv4977705copy number variation1nstd200human GRCh38 chr10: 132,786,266-132,786,465 , GRCh37.p13 chr10: 134,599,770-134,599,969 NKX6-2
    nsv4830765copy number variation1nstd200human GRCh37 chr10: 134,566,045-134,762,186 , GRCh38.p12 chr10: 132,752,541-132,948,682 NKX6-2, LOC105378572, 4 more genes
    nsv4729670copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,031,265-135,427,143 , GRCh38.p12 chr10: 127,233,001-133,613,639 LOC105378561, LINC01164, 91 more genes
    nsv4676098copy number variation1nstd102humanUncertain significance GRCh37 chr10: 134,184,419-135,095,908 , GRCh38.p12 chr10: 132,370,915-133,282,404 VENTX, RPL5P28, 26 more genes
    nsv4676007copy number variation1nstd102humanUncertain significance GRCh37 chr10: 134,182,977-134,624,664 , GRCh38.p12 chr10: 132,369,473-132,811,160 LINC02870, LINC03068, 7 more genes
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4675508copy number variation1nstd102humanLikely benign GRCh37 chr10: 134,589,739-134,868,301 , GRCh38.p12 chr10: 132,776,235-133,054,797 INPP5A, LOC107984283, 8 more genes
    nsv4675355copy number variation1nstd102humanUncertain significance GRCh37 chr10: 134,213,086-134,693,934 , GRCh38.p12 chr10: 132,399,582-132,880,430 LINC03068, LOC105378571, 7 more genes
    nsv4675230copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,009,772-135,427,143 , GRCh38.p12 chr10: 127,211,508-133,613,639 EBF3-AS1, LINC02646, 91 more genes
    nsv4674901copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,381,095-135,427,143 , GRCh38.p12 chr10: 127,582,831-133,613,639 LOC100419870, MIR378C, 88 more genes
    nsv4617387copy number variation1nstd183human GRCh37 chr10: 132,132,586-134,972,183 , GRCh38.p12 chr10: 130,334,322-133,158,679 , LOC105378572, 37 more genes
    nsv4609845copy number variation1nstd183human GRCh37 chr10: 134,598,567-134,599,192 , GRCh38.p12 chr10: 132,785,063-132,785,688 NKX6-2
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