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Items: 1 to 20 of 359

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv5954523copy number variation1nstd209human GRCh38 chr21: 38,063,960-38,064,167 , GRCh37.p13 chr: NaN-NaN DSCR4
    nsv5712731mobile element insertion1nstd211human GRCh38 chr21: 38,082,127-38,082,127 , GRCh37.p13 chr21: 39,454,221-39,454,221 DSCR4
    nsv5669144insertion1nstd207human GRCh38 chr21: 38,059,628-38,059,628 , GRCh37.p13 chr21: 39,431,930-39,431,930 DSCR4
    nsv5591690copy number variation1nstd207human GRCh38 chr21: 38,063,960-38,064,167 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN DSCR4
    nsv5589428copy number variation1nstd207human GRCh38 chr21: 38,109,100-38,109,469 , GRCh37.p13 chr21: 39,481,194-39,481,563 DSCR4
    nsv5551448copy number variation1nstd206human GRCh38 chr21: 38,063,910-38,064,168 , GRCh37.p13 chr: NaN-NaN DSCR4
    nsv5543667copy number variation1nstd206human GRCh38 chr21: 38,068,663-38,069,102 , GRCh37.p13 chr21: 39,440,757-39,441,196 DSCR4
    nsv5539790insertion1nstd206human GRCh38 chr21: 5,227,438-39,583,816 , GRCh37.p13 chr21: 10,697,897-44,966,043 , LOC100419041, 557 more genes
    nsv5160316mobile element insertion1nstd203human GRCh38 chr21: 38,068,325-38,068,344 , GRCh37.p13 chr21: 39,440,419-39,440,438 DSCR4
    nsv5029002copy number variation1nstd200human GRCh38 chr21: 38,114,952-38,115,095 , GRCh37.p13 chr21: 39,487,046-39,487,189 DSCR4
    nsv5029001copy number variation1nstd200human GRCh38 chr21: 38,080,518-38,089,736 , GRCh37.p13 chr21: 39,452,612-39,461,830 DSCR4
    nsv4863238copy number variation1nstd200human GRCh37 chr21: 39,452,612-39,461,830 , GRCh38.p12 chr21: 38,080,518-38,089,736 DSCR4
    nsv4768387copy number variation1nstd102humanPathogenic NCBI36 chr21: 37,662,974-39,195,976 , GRCh37.p13 chr21: 38,741,104-40,274,106 , GRCh38.p12 chr21: 37,368,802-38,902,182 SNRPGP13, LOC105372797, 22 more genes
    nsv4768385copy number variation1nstd102humanPathogenic NCBI36 chr21: 37,662,974-39,236,719 , GRCh37.p13 chr21: 38,741,104-40,314,849 , GRCh38.p12 chr21: 37,368,802-38,942,925 DYRK1A, LOC100288590, 22 more genes
    nsv4756784insertion1nstd199human GRCh37 chr21: 39,431,928-39,431,928 , GRCh38.p12 chr21: 38,059,626-38,059,626 DSCR4
    nsv4736223copy number variation1nstd199human GRCh37 chr21: 39,481,463-39,481,830 , GRCh38.p12 chr21: 38,109,369-38,109,736 DSCR4
    nsv4730021copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,629,063-48,090,317 , GRCh38.p12 chr21: 13,256,742-46,670,405 SLX9, LOC105372750, 619 more genes
    nsv4729836copy number variation1nstd102humanUncertain significance GRCh37 chr21: 39,270,345-41,091,831 , GRCh38.p12 chr21: 37,898,042-39,719,904 ERG, DSCR8, 43 more genes
    nsv4679058copy number variation1nstd189human GRCh37.p13 chr21: 14,468,835-48,129,895 , GRCh38.p12 chr21: 13,096,514-46,699,983 , ADARB1, 652 more genes
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