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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5961695insertion1nstd209human GRCh38 chr5: 39,423,334-39,423,334 , GRCh37.p13 chr5: 39,423,436-39,423,436 DAB2
    nsv5892204copy number variation1nstd209human GRCh38 chr5: 39,374,241-39,374,374 , GRCh37.p13 chr5: 39,374,343-39,374,476 DAB2
    nsv5638888insertion1nstd207human GRCh38 chr5: 39,423,334-39,423,334 , GRCh37.p13 chr5: 39,423,436-39,423,436 DAB2
    nsv5568938copy number variation1nstd207human GRCh38 chr5: 39,374,241-39,374,374 , GRCh37.p13 chr5: 39,374,343-39,374,476 DAB2
    nsv5539313insertion1nstd206human GRCh38 chr5: 39,423,337-39,423,385 , GRCh37.p13 chr5: 39,423,439-39,423,487 DAB2
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5459791copy number variation1nstd206human GRCh38 chr5: 39,374,241-39,374,375 , GRCh37.p13 chr5: 39,374,343-39,374,477 DAB2
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5356358translocation1nstd200human GRCh38 chr1: 235,718,597-235,718,597 , GRCh38 chr5: 39,402,581-39,402,581 , GRCh37.p13 chr1: 235,881,897-235,881,897 , GRCh37.p13 chr5: 39,402,683-39,402,683 DAB2, LYST
    nsv5170168mobile element insertion1nstd203human GRCh38 chr5: 39,409,800-39,409,816 , GRCh37.p13 chr5: 39,409,902-39,409,918 DAB2
    nsv4946726copy number variation1nstd200human GRCh38 chr5: 39,407,693-39,411,156 , GRCh37.p13 chr5: 39,407,795-39,411,258 DAB2
    nsv4946725copy number variation1nstd200human GRCh38 chr5: 39,374,241-39,374,375 , GRCh37.p13 chr5: 39,374,343-39,374,477 DAB2
    nsv4802579copy number variation1nstd200human GRCh37 chr5: 39,407,795-39,411,258 , GRCh38.p12 chr5: 39,407,693-39,411,156 DAB2
    nsv4754343insertion1nstd199human GRCh37 chr5: 39,423,435-39,423,435 , GRCh38.p12 chr5: 39,423,333-39,423,333 DAB2
    nsv4721883insertion1nstd186human GRCh37 chr5: 39,423,436-39,423,436 , GRCh38.p12 chr5: 39,423,334-39,423,334 DAB2
    nsv4680426copy number variation1nstd189human GRCh37.p13 chr5: 37,623,394-42,403,769 , GRCh38.p12 chr5: 37,623,292-42,403,667 , C6, 65 more genes
    nsv4674231copy number variation1nstd102humanPathogenic GRCh37 chr5: 38,432,180-49,441,945 , GRCh38.p12 chr5: 38,432,078-50,146,111 RPSAP38, LOC105374746, 92 more genes
    nsv4646696copy number variation2nstd186human GRCh37 chr5: 39,374,343-39,374,477 , GRCh38.p12 chr5: 39,374,241-39,374,375 DAB2
    nsv4639058copy number variation1nstd186human GRCh37 chr5: 39,374,344-39,374,477 , GRCh38.p12 chr5: 39,374,242-39,374,375 DAB2
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