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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5843689copy number variation1nstd209human GRCh38 chr6: 10,672,417-10,674,216 , GRCh37.p13 chr6: 10,672,650-10,674,449 , C6orf52
    nsv5843640copy number variation1nstd209human GRCh38 chr6: 10,670,417-10,671,416 , GRCh37.p13 chr6: 10,670,650-10,671,649 , C6orf52
    nsv5683510mobile element insertion1nstd211human GRCh38 chr6: 10,682,942-10,682,942 , GRCh37.p13 chr6: 10,683,175-10,683,175 , C6orf52, 1 more genes
    nsv5471687copy number variation1nstd206human GRCh38 chr6: 10,692,364-10,692,441 , GRCh37.p13 chr6: 10,692,597-10,692,674 PAK1IP1, C6orf52
    nsv5381380copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,556,657-10,775,712 , GRCh38.p12 chr6: 10,556,424-10,775,479 , GRCh38.p12 chr6|NW_018654713.1: 67,308-242,796 GCNT2P1, MAK, 7 more genes
    nsv5226653copy number variation1nstd204human GRCh38.p13 chr6: 10,675,917-10,678,916 , GRCh37.p13 chr6: 10,676,150-10,679,149 , C6orf52
    nsv4947775copy number variation1nstd200human GRCh38 chr6: 10,677,389-10,677,477 , GRCh37.p13 chr6: 10,677,622-10,677,710 , C6orf52
    nsv4947774copy number variation1nstd200human GRCh38 chr6: 10,669,742-10,673,847 , GRCh37.p13 chr6: 10,669,975-10,674,080 , C6orf52
    nsv4947748copy number variation1nstd200human GRCh38 chr6: 10,465,448-10,718,419 , GRCh37.p13 chr6: 10,465,681-10,718,652 , LOC101928146, 8 more genes
    nsv4934417copy number variation1nstd200human GRCh38 chr6: 10,694,369-10,713,817 , GRCh37.p13 chr6: 10,694,602-10,714,050 C6orf52, PAK1IP1
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
    nsv4734285copy number variation1nstd199human GRCh37 chr6: 10,676,093-10,681,701 , GRCh38.p12 chr6: 10,675,860-10,681,468 , GRCh38.p12 chr6|NW_018654713.1: 186,744-192,352 , C6orf52
    nsv4729108copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,514,491-10,677,096 , GRCh38.p12 chr6: 10,514,258-10,676,863 , GRCh38.p12 chr6|NW_018654713.1: 25,142-187,747 GCNT2P1, RPL21P63, 4 more genes
    nsv4683407copy number variation1nstd102humanUncertain significance GRCh37 chr6: 10,393,732-11,011,042 , GRCh38.p12 chr6: 10,393,499-11,010,809 MAK, TMEM14C, 22 more genes
    nsv4523207copy number variation1nstd166human GRCh37.p13 chr6: 10,677,622-10,677,710 , GRCh38.p12 chr6: 10,677,389-10,677,477 , GRCh38.p12 chr6|NW_018654713.1: 188,273-188,361 , C6orf52
    nsv4486440mobile element insertion1nstd166human GRCh37.p13 chr6: 10,683,159-10,683,159 , GRCh38.p12 chr6: 10,682,926-10,682,926 , GRCh38.p12 chr6|NW_018654713.1: 193,810-193,810 , C6orf52, 1 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4131259copy number variation1nstd166human GRCh37.p13 chr6: 10,659,000-10,676,000 , GRCh38.p12 chr6: 10,658,767-10,675,767 , GRCh38.p12 chr6|NW_018654713.1: 169,651-186,651 , C6orf52
    nsv4123212copy number variation1nstd166human GRCh37.p13 chr6: 10,676,097-10,681,702 , GRCh38.p12 chr6|NW_018654713.1: 186,748-192,353 , GRCh38.p12 chr6: 10,675,864-10,681,469 , C6orf52
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
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