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Items: 1 to 20 of 389

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120330copy number variation1nstd186human GRCh37 chr5: 141,976,241-141,976,343 , GRCh38.p12 chr5: 142,596,676-142,596,778 FGF1
    nsv5960833insertion1nstd209human GRCh38 chr5: 142,656,218-142,656,218 , GRCh37.p13 chr5: 142,035,783-142,035,783 FGF1
    nsv5955180insertion1nstd209human GRCh38 chr5: 142,692,703-142,692,703 , GRCh37.p13 chr5: 142,072,268-142,072,268 FGF1
    nsv5905450copy number variation1nstd209human GRCh38 chr5: 142,596,674-142,596,777 , GRCh37.p13 chr5: 141,976,239-141,976,342 FGF1
    nsv5896290copy number variation1nstd209human GRCh38 chr5: 142,636,655-142,641,937 , GRCh37.p13 chr5: 142,016,220-142,021,502 FGF1
    nsv5892386copy number variation1nstd209human GRCh38 chr5: 142,646,188-142,646,770 , GRCh37.p13 chr5: 142,025,753-142,026,335 FGF1
    nsv5891040copy number variation1nstd209human GRCh38 chr5: 142,622,914-142,623,873 , GRCh37.p13 chr5: 142,002,479-142,003,438 FGF1
    nsv5889547copy number variation1nstd209human GRCh38 chr5: 142,615,486-142,619,063 , GRCh37.p13 chr5: 141,995,051-141,998,628 FGF1
    nsv5841459copy number variation1nstd209human GRCh38 chr5: 142,636,639-142,641,974 , GRCh37.p13 chr5: 142,016,204-142,021,539 FGF1
    nsv5841163copy number variation1nstd209human GRCh38 chr5: 142,615,420-142,619,048 , GRCh37.p13 chr5: 141,994,985-141,998,613 FGF1
    nsv5727195mobile element insertion1nstd211human GRCh38 chr5: 142,640,680-142,640,680 , GRCh37.p13 chr5: 142,020,245-142,020,245 FGF1
    nsv5682199mobile element insertion2nstd211human GRCh38 chr5: 142,615,047-142,615,047 , GRCh37.p13 chr5: 141,994,612-141,994,612 FGF1
    nsv5681279mobile element insertion2nstd211human GRCh38 chr5: 142,656,235-142,656,235 , GRCh37.p13 chr5: 142,035,800-142,035,800 FGF1
    nsv5641817insertion1nstd207human GRCh38 chr5: 142,596,352-142,596,352 , GRCh37.p13 chr5: 141,975,917-141,975,917 FGF1
    nsv5637921insertion1nstd207human GRCh38 chr5: 142,656,218-142,656,218 , GRCh37.p13 chr5: 142,035,783-142,035,783 FGF1
    nsv5583298copy number variation1nstd207human GRCh38 chr5: 142,596,674-142,596,777 , GRCh37.p13 chr5: 141,976,239-141,976,342 FGF1
    nsv5579977copy number variation1nstd207human GRCh38 chr5: 142,646,018-142,646,302 , GRCh37.p13 chr5: 142,025,583-142,025,867 FGF1
    nsv5569314copy number variation1nstd207human GRCh38 chr5: 142,596,308-142,596,443 , GRCh37.p13 chr5: 141,975,873-141,976,008 FGF1
    nsv5470645copy number variation1nstd206human GRCh38 chr5: 142,641,743-142,641,829 , GRCh37.p13 chr5: 142,021,308-142,021,394 FGF1
    nsv5470145copy number variation1nstd206human GRCh38 chr5: 142,429,551-143,065,626 , GRCh37.p13 chr5: 141,809,116-142,445,191 FGF1, ARHGAP26, 5 more genes
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