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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5725123mobile element insertion1nstd211human GRCh38 chr6: 89,362,086-89,362,086 , GRCh37.p13 chr6: 90,071,805-90,071,805 RRAGD
    nsv5557176mobile element insertion1nstd206human GRCh38 chr6: 89,362,086-89,362,137 , GRCh37.p13 chr6: 90,071,805-90,071,856 RRAGD
    nsv5460686copy number variation1nstd206human GRCh38 chr6: 89,401,453-89,402,280 , GRCh37.p13 chr6: 90,111,172-90,111,999 RRAGD
    nsv5101432mobile element insertion1nstd203human GRCh38 chr6: 89,364,892-89,364,905 , GRCh37.p13 chr6: 90,074,611-90,074,624 RRAGD
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4942069copy number variation1nstd200human GRCh38 chr6: 89,399,887-89,402,298 , GRCh37.p13 chr6: 90,109,606-90,112,017 RRAGD
    nsv4942068copy number variation1nstd200human GRCh38 chr6: 89,386,471-89,387,160 , GRCh37.p13 chr6: 90,096,190-90,096,879 RRAGD
    nsv4824538copy number variation1nstd200human GRCh37 chr6: 90,094,412-90,094,664 , GRCh38.p12 chr6: 89,384,693-89,384,945 RRAGD
    nsv4816949copy number variation1nstd200human GRCh37 chr6: 90,109,606-90,112,017 , GRCh38.p12 chr6: 89,399,887-89,402,298 RRAGD
    nsv4728930copy number variation1nstd102humanUncertain significance GRCh37 chr6: 90,085,893-90,910,484 , GRCh38.p12 chr6: 89,376,174-90,200,765 RRAGD, MDN1-AS1, 15 more genes
    nsv4675498copy number variation1nstd102humanUncertain significance GRCh37 chr6: 90,108,876-90,806,063 , GRCh38.p12 chr6: 89,399,157-90,096,344 RN7SL11P, LOC105377889, 14 more genes
    nsv4566803mobile element insertion1nstd166human GRCh37.p13 chr6: 90,102,963-90,102,963 , GRCh38.p12 chr6: 89,393,244-89,393,244 RRAGD
    nsv4494074mobile element insertion1nstd166human GRCh37.p13 chr6: 90,085,816-90,085,816 , GRCh38.p12 chr6: 89,376,097-89,376,097 RRAGD
    nsv4478855mobile element insertion1nstd166human GRCh37.p13 chr6: 90,080,445-90,080,445 , GRCh38.p12 chr6: 89,370,726-89,370,726 RRAGD
    nsv4456405copy number variation1nstd102humanUncertain significance GRCh37 chr6: 87,627,836-93,698,486 , GRCh38.p12 chr6: 86,918,118-92,988,768 MIR4643, LOC107986625, 82 more genes
    nsv4455227copy number variation1nstd102humanUncertain significance GRCh37 chr6: 88,783,642-96,282,103 , GRCh38.p12 chr6: 88,073,924-95,834,227 MDN1, DNAJC19P6, 65 more genes
    nsv4140789copy number variation1nstd166human GRCh37.p13 chr6: 90,072,068-90,074,630 , GRCh38.p12 chr6: 89,362,349-89,364,911 RRAGD
    nsv4140756copy number variation1nstd166human GRCh37.p13 chr6: 90,094,412-90,094,663 , GRCh38.p12 chr6: 89,384,693-89,384,944 RRAGD
    nsv3923528copy number variation1nstd102humanPathogenic NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189 RNU4-72P, LOC100132830, 157 more genes
    nsv3922502copy number variation1nstd102humanUncertain significance NCBI36 chr6: 89,774,237-90,472,036 , GRCh37 chr6: 89,717,518-90,415,315 , GRCh38 chr6: 89,007,799-89,705,596 RN7SL11P, LOC105377889, 17 more genes
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