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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140530insertion1nstd232human GRCh37.p13 chr7: 54,825,289-54,825,289 , GRCh38.p12 chr7: 54,757,596-54,757,596 SEC61G, SEC61G-DT
    nsv7057571inversion1nstd229human GRCh38 chr7: 54,577,199-54,892,594 , GRCh37.p13 chr7: 54,644,892-54,960,287 RPL31P35, SEC61G, 2 more genes
    nsv6836722copy number variation1nstd229human GRCh38 chr7: 51,354,950-55,353,996 , GRCh37.p13 chr7: 51,422,647-55,421,689 GS1-278J22.2, RNF138P2, 41 more genes
    nsv6826812copy number variation1nstd229human GRCh38 chr7: 54,749,571-54,755,877 , GRCh37.p13 chr7: 54,817,264-54,823,570 SEC61G
    nsv6822841copy number variation1nstd229human GRCh38 chr7: 54,756,101-54,769,400 , GRCh37.p13 chr7: 54,823,794-54,837,093 SEC61G, SEC61G-DT
    nsv6820007copy number variation1nstd229human GRCh38 chr7: 54,577,201-55,098,300 , GRCh37.p13 chr7: 54,644,894-55,165,993 LOC105375284, SEC61G-DT, 5 more genes
    nsv6636595copy number variation1nstd102humanUncertain significance GRCh37 chr7: 53,991,820-56,148,011 , GRCh38.p12 chr7: 53,924,127-56,080,318 PSPH, SNORA22B, 46 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6601253copy number variation1nstd223human GRCh38 chr7: 54,583,600-55,152,153 , GRCh37.p13 chr7: 54,651,293-55,219,846 EGFR, LOC105375284, 5 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6136192copy number variation1nstd213human GRCh37 chr7: 54,300,000-56,060,001 , GRCh38.p12 chr7: 54,232,307-55,992,308 EGFR, SLC25A5P3, 39 more genes
    nsv6017873copy number variation1nstd212human GRCh38 chr7: 54,759,207-54,759,452 , GRCh37.p13 chr7: 54,826,900-54,827,145 SEC61G, SEC61G-DT
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5484015copy number variation1nstd206human GRCh38 chr7: 54,754,647-54,754,722 , GRCh37.p13 chr7: 54,822,340-54,822,415 SEC61G
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4953710copy number variation1nstd200human GRCh38 chr7: 54,583,600-55,152,153 , GRCh37.p13 chr7: 54,651,293-55,219,846 SEC61G, SEC61G-DT, 5 more genes
    nsv4828951copy number variation1nstd200human GRCh37 chr7: 54,651,293-55,219,846 , GRCh38.p12 chr7: 54,583,600-55,152,153 EGFR, LOC643168, 5 more genes
    nsv4457295copy number variation1nstd102humanUncertain significance GRCh37 chr7: 54,644,022-55,165,236 , GRCh38.p12 chr7: 54,576,329-55,097,543 RNU6-1125P, SEC61G, 5 more genes
    nsv4456853copy number variation1nstd102humanUncertain significance GRCh37 chr7: 54,651,292-55,220,177 , GRCh38.p12 chr7: 54,583,599-55,152,484 RPL31P35, RNU6-1125P, 5 more genes
    nsv4455806copy number variation1nstd102humanUncertain significance GRCh37 chr7: 52,809,787-58,025,873 , GRCh38.p12 chr7: 52,742,093-57,966,167 RPL31P35, SEC61G, 161 more genes
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