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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5898554copy number variation1nstd209human GRCh38 chr6: 159,797,716-159,797,956 , GRCh37.p13 chr6: 160,218,748-160,218,988 PNLDC1, MRPL18
    nsv5892607copy number variation1nstd209human GRCh38 chr6: 159,796,294-159,796,369 , GRCh37.p13 chr6: 160,217,326-160,217,401 MRPL18
    nsv5473551copy number variation1nstd206human GRCh38 chr6: 159,796,295-159,796,370 , GRCh37.p13 chr6: 160,217,327-160,217,402 MRPL18
    nsv5343693translocation1nstd200human GRCh37 chr6: 160,218,989-160,218,989 , GRCh37 chr6: 160,218,751-160,218,751 , GRCh38.p12 chr6: 159,797,719-159,797,719 , GRCh38.p12 chr6: 159,797,957-159,797,957 PNLDC1, MRPL18
    nsv5339181translocation1nstd200human GRCh37 chr1: 43,823,171-43,823,171 , GRCh37 chr6: 160,210,698-160,210,698 , GRCh38.p12 chr1: 43,357,500-43,357,500 , GRCh38.p12 chr6: 159,789,666-159,789,666 CDC20, TCP1, 2 more genes
    nsv5310684copy number variation1nstd204human GRCh38.p13 chr6: 159,734,848-159,969,288 , GRCh37.p13 chr6: 160,155,880-160,390,320 SNORA29, SOD2-OT1, 9 more genes
    nsv5221863copy number variation1nstd204human GRCh38.p13 chr6: 159,734,701-159,927,700 , GRCh37.p13 chr6: 160,155,733-160,348,732 PNLDC1, SNORA20, 8 more genes
    nsv4824839copy number variation1nstd200human GRCh37 chr6: 160,155,890-160,390,316 , GRCh38.p12 chr6: 159,734,858-159,969,284 SNORA29, MRPL18, 9 more genes
    nsv4766814inversion1nstd199human GRCh37 chr6: 153,752,140-161,206,728 , GRCh38.p12 chr6: 153,431,005-160,785,696 , ACAT2, 111 more genes
    nsv4729113copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,998,877-160,413,982 , GRCh38.p12 chr6: 159,577,845-159,992,950 PNLDC1, MRPL18, 12 more genes
    nsv4604362copy number variation1nstd183human GRCh37 chr6: 160,211,263-160,211,748 , GRCh38.p12 chr6: 159,790,231-159,790,716 MRPL18
    nsv4566801mobile element insertion1nstd166human GRCh37.p13 chr6: 160,210,060-160,210,060 , GRCh38.p12 chr6: 159,789,028-159,789,028 MRPL18, TCP1
    nsv4456598copy number variation1nstd102humanUncertain significance GRCh37 chr6: 160,025,206-160,271,483 , GRCh38.p12 chr6: 159,604,174-159,850,451 SOD2-OT1, RNU4ATAC18P, 10 more genes
    nsv4455446copy number variation1nstd102humanUncertain significance GRCh37 chr6: 157,262,571-160,992,289 , GRCh38.p12 chr6: 156,941,437-160,571,257 LOC105378076, LOC107986663, 67 more genes
    nsv4436131complex substitution1nstd102humanPathogenic GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067 ACAT2, CCR6, 303 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4149977copy number variation1nstd166human GRCh37.p13 chr6: 160,210,684-160,211,365 , GRCh38.p12 chr6: 159,789,652-159,790,333 MRPL18, TCP1
    nsv3921695copy number variation1nstd102humanPathogenic GRCh38 chr6: 154,539,655-170,714,507 , NCBI36 chr6: 154,902,481-170,865,520 , GRCh37 chr6: 154,860,789-171,023,595 LOC105378128, LOC105378102, 255 more genes
    nsv3921491copy number variation1nstd102humanPathogenic NCBI36 chr6: 159,795,661-170,763,014 , GRCh38 chr6: 159,454,639-170,612,001 , GRCh37 chr6: 159,875,671-170,921,089 LOC102724357, LOC101929142, 183 more genes
    nsv3920975copy number variation1nstd102humanPathogenic GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591 UST-AS2, LOC729681, 394 more genes
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