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Items: 1 to 20 of 558

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137168copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,771,367-68,835,572 , GRCh38.p12 chr16: 68,737,464-68,801,669 CDH1, RNA5SP429
    nsv7137072copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 68,737,292-68,737,463 , GRCh37.p13 chr16: 68,771,195-68,771,366 CDH1
    nsv7137069copy number variation1nstd102humanPathogenic GRCh38 chr16: 68,737,292-68,835,537 , GRCh37.p13 chr16: 68,771,195-68,869,440 RNA5SP429, CDH1, 1 more genes
    nsv7137066copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 68,833,290-68,835,537 , GRCh37.p13 chr16: 68,867,193-68,869,440 CDH1
    nsv7137060copy number variation1nstd102humanUncertain significance GRCh37 chr16: 68,801,456-68,805,169 , GRCh38 chr16: 68,767,553-68,771,266 CDH1
    nsv7137057copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 68,866,797-68,867,625 , GRCh38 chr16: 68,832,894-68,833,722 CDH1
    nsv7137043copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 68,845,110-68,846,752 , GRCh38 chr16: 68,811,207-68,812,849 CDH1
    nsv7137042copy number variation1nstd102humanUncertain significance GRCh37 chr16: 68,828,992-68,833,614 , GRCh38 chr16: 68,795,089-68,799,711 CDH1
    nsv7094859copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,853,173-68,853,338 , GRCh38.p12 chr16: 68,819,270-68,819,435 CDH1
    nsv7094858copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,845,577-68,849,672 , GRCh38.p12 chr16: 68,811,674-68,815,769 CDH1
    nsv7094857copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 68,842,317-68,849,672 , GRCh38.p12 chr16: 68,808,414-68,815,769 CDH1
    nsv7094688copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,861,950-68,863,561 , GRCh38.p12 chr16: 68,828,047-68,829,658 CDH1
    nsv7094685copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,710,268-68,867,402 , GRCh38.p12 chr16: 68,676,365-68,833,499 CDH3, RNA5SP429, 3 more genes
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7094592copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 68,842,317-68,853,338 , GRCh38.p12 chr16: 68,808,414-68,819,435 CDH1
    nsv7094591copy number variation1nstd102humanUncertain significance GRCh37 chr16: 68,679,283-68,857,549 , GRCh38.p12 chr16: 68,645,380-68,823,646 RNA5SP429, FTLP14, 4 more genes
    nsv7075094inversion1nstd229human GRCh38 chr16: 67,913,190-69,541,641 , GRCh37.p13 chr16: 67,947,093-69,575,544 PSMB10, COG8, 52 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6995954copy number variation1nstd229human GRCh38 chr16: 68,794,186-68,797,203 , GRCh37.p13 chr16: 68,828,089-68,831,106 CDH1
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