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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097826copy number variation1nstd102humanPathogenic GRCh37 chr6: 41,126,341-43,752,536 , GRCh38.p12 chr6: 41,158,603-43,784,799 USP49, PRICKLE4, 96 more genes
    nsv7097825copy number variation1nstd102humanUncertain significance GRCh37 chr6: 41,126,341-43,737,486 , GRCh38.p12 chr6: 41,158,603-43,769,749 DNPH1, LOC107986596, 96 more genes
    nsv7097331copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,162,409-44,154,249 , GRCh38.p12 chr6: 42,194,671-44,186,512 MRPS10, CUL9, 70 more genes
    nsv6796074copy number variation1nstd229human GRCh38 chr6: 43,642,251-43,647,173 , GRCh37.p13 chr6: 43,609,988-43,614,910 RSPH9
    nsv6793547copy number variation1nstd229human GRCh38 chr6: 43,644,435-43,677,116 , GRCh37.p13 chr6: 43,612,172-43,644,853 RSPH9, MRPS18A
    nsv6791704copy number variation1nstd229human GRCh38 chr6: 42,737,001-44,115,000 , GRCh37.p13 chr6: 42,704,739-44,082,737 ZNF318, RPL24P4, 56 more genes
    nsv6788343copy number variation1nstd229human GRCh38 chr6: 43,624,808-43,734,661 , GRCh37.p13 chr6: 43,592,545-43,702,398 MRPS18A, RSPH9, 3 more genes
    nsv6786386copy number variation1nstd229human GRCh38 chr6: 43,484,801-43,798,200 , GRCh37.p13 chr6: 43,452,539-43,765,937 POLH, LRRC73, 12 more genes
    nsv6783168copy number variation1nstd229human GRCh38 chr6: 43,339,401-43,752,100 , GRCh37.p13 chr6: 43,307,139-43,719,837 MRPS18A, RNU6-1113P, 17 more genes
    nsv6782730copy number variation1nstd229human GRCh38 chr6: 43,663,173-43,675,181 , GRCh37.p13 chr6: 43,630,910-43,642,918 RSPH9, MRPS18A
    nsv6781131copy number variation1nstd229human GRCh38 chr6: 43,660,025-43,662,658 , GRCh37.p13 chr6: 43,627,762-43,630,395 RSPH9
    nsv6778462copy number variation1nstd229human GRCh38 chr6: 43,647,112-43,647,174 , GRCh37.p13 chr6: 43,614,849-43,614,911 RSPH9
    nsv6636332copy number variation1nstd102humanUncertain significance GRCh37 chr6: 43,571,555-44,154,599 , GRCh38.p12 chr6: 43,603,818-44,186,862 CAPN11, LOC105375068, 18 more genes
    nsv6631415copy number variation1nstd224human GRCh37 chr6: 43,401,090-43,719,993 , GRCh38.p12 chr6: 43,433,352-43,752,256 POLH, MAD2L1BP, 14 more genes
    nsv6566770inversion1nstd223human GRCh38 chr6: 42,194,666-44,186,502 , GRCh37.p13 chr6: 42,162,404-44,154,239 RPL36AP5, MIR6780B, 70 more genes
    nsv6400810copy number variation1nstd223human GRCh38 chr6: 43,405,006-43,758,997 , GRCh37.p13 chr6: 43,372,744-43,726,734 MIR6780B, LOC105375065, 15 more genes
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6170710copy number variation1nstd214human GRCh38 chr6: 43,647,109-43,647,173 , GRCh37.p13 chr6: 43,614,846-43,614,910 RSPH9
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6135515copy number variation1nstd213human GRCh37 chr6: 43,220,000-44,970,001 , GRCh38.p12 chr6: 43,252,262-45,002,264 SLC29A1, NFKBIE, 54 more genes
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