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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7141328insertion1nstd232human GRCh37.p13 chr7: 140,374,557-140,374,557 , GRCh38.p12 chr7: 140,674,757-140,674,757 ADCK2
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7097607copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 138,391,369-141,759,786 , GRCh38.p12 chr7: 138,706,624-142,059,986 LOC105375535, AGK-DT, 82 more genes
    nsv7047243inversion1nstd229human GRCh38 chr7: 140,412,248-142,426,166 , GRCh37.p13 chr7: 140,112,048-142,048,195 OR9A4, AGK-DT, 69 more genes
    nsv7044890inversion1nstd229human GRCh38 chr7: 140,412,271-142,426,160 , GRCh37.p13 chr7: 140,112,071-142,048,195 WEE2, LOC105375535, 69 more genes
    nsv7040689inversion1nstd229human GRCh38 chr7: 140,412,886-142,426,274 , GRCh37.p13 chr7: 140,112,686-142,048,195 MYL6P4, TMEM178B, 69 more genes
    nsv6837649copy number variation1nstd229human GRCh38 chr7: 140,654,601-140,706,500 , GRCh37.p13 chr7: 140,354,401-140,406,300 NDUFB2-AS1, ADCK2, 1 more genes
    nsv6834078copy number variation1nstd229human GRCh38 chr7: 140,684,070-140,687,648 , GRCh37.p13 chr7: 140,383,870-140,387,448 ADCK2
    nsv6834058copy number variation1nstd229human GRCh38 chr7: 140,694,526-140,719,873 , GRCh37.p13 chr7: 140,394,326-140,419,673 ADCK2, NDUFB2, 2 more genes
    nsv6829978copy number variation1nstd229human GRCh38 chr7: 140,016,565-141,119,379 , GRCh37.p13 chr7: 139,716,365-140,819,179 KDM7A, LOC107986854, 29 more genes
    nsv6828146copy number variation1nstd229human GRCh38 chr7: 140,682,148-140,685,998 , GRCh37.p13 chr7: 140,381,948-140,385,798 ADCK2
    nsv6827454copy number variation1nstd229human GRCh38 chr7: 140,685,188-140,844,191 , GRCh37.p13 chr7: 140,384,988-140,543,991 NDUFB2-AS1, ADCK2, 2 more genes
    nsv6822835copy number variation1nstd229human GRCh38 chr7: 140,685,613-140,688,977 , GRCh37.p13 chr7: 140,385,413-140,388,777 ADCK2
    nsv6818329copy number variation1nstd229human GRCh38 chr7: 140,386,553-140,693,349 , GRCh37.p13 chr7: 140,086,353-140,393,149 LOC642355, NDUFB2-AS1, 8 more genes
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 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
    nsv6429334copy number variation1nstd223human GRCh38 chr7: 140,016,565-141,119,379 , GRCh37.p13 chr7: 139,716,365-140,819,179 LOC105375534, PPP1R2P6, 29 more genes
    nsv6420378copy number variation1nstd223human GRCh38 chr7: 140,672,601-140,674,300 , GRCh37.p13 chr7: 140,372,401-140,374,100 ADCK2
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