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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6992671copy number variation1nstd229human GRCh38 chr17: 58,527,867-58,531,399 , GRCh37.p13 chr17: 56,605,228-56,608,760 SEPTIN4-AS1, SEPTIN4
    nsv6987320copy number variation1nstd229human GRCh38 chr17: 58,526,235-58,526,413 , GRCh37.p13 chr17: 56,603,596-56,603,774 SEPTIN4, SEPTIN4-AS1
    nsv6985907copy number variation1nstd229human GRCh38 chr17: 58,526,258-58,531,839 , GRCh37.p13 chr17: 56,603,619-56,609,200 SEPTIN4-AS1, SEPTIN4
    nsv6984598copy number variation1nstd229human GRCh38 chr17: 58,542,080-58,875,342 , GRCh37.p13 chr17: 56,619,441-56,952,703 LOC107985048, RNU1-108P, 11 more genes
    nsv6634423copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,043,662-56,728,123 , GRCh38.p12 chr17: 56,966,301-58,650,762 RNU7-134P, DYNLL2-DT, 42 more genes
    nsv6516573copy number variation1nstd223human GRCh38 chr17: 58,532,672-58,534,089 , GRCh37.p13 chr17: 56,610,033-56,611,450 SEPTIN4, SEPTIN4-AS1
    nsv6310393copy number variation1nstd102humanUncertain significance GRCh37 chr17: 54,671,585-59,938,900 , GRCh38.p12 chr17: 56,594,224-61,861,539 RNF43, LOC107985048, 132 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5531844copy number variation1nstd206human GRCh38 chr17: 58,531,853-58,532,031 , GRCh37.p13 chr17: 56,609,214-56,609,392 SEPTIN4-AS1, SEPTIN4
    nsv5530743copy number variation1nstd206human GRCh38 chr17: 58,520,361-58,525,117 , GRCh37.p13 chr17: 56,597,722-56,602,478 SEPTIN4, SEPTIN4-AS1
    nsv5520588copy number variation1nstd206human GRCh38 chr17: 58,536,789-58,555,082 , GRCh37.p13 chr17: 56,614,150-56,632,443 SEPTIN4, TEX14, 1 more genes
    nsv5381036copy number variation1nstd102humanUncertain significance GRCh37 chr17: 56,432,304-56,811,583 , GRCh38.p12 chr17: 58,354,943-58,734,222 SEPTIN4-AS1, MTMR4, 13 more genes
    nsv5285865copy number variation1nstd204human GRCh38.p13 chr17: 58,520,098-58,522,547 , GRCh37.p13 chr17: 56,597,459-56,599,908 SEPTIN4, SEPTIN4-AS1
    nsv5010369copy number variation1nstd200human GRCh38 chr17: 58,532,672-58,534,089 , GRCh37.p13 chr17: 56,610,033-56,611,450 SEPTIN4, SEPTIN4-AS1
    nsv5010368copy number variation1nstd200human GRCh38 chr17: 58,531,905-58,532,005 , GRCh37.p13 chr17: 56,609,266-56,609,366 SEPTIN4-AS1, SEPTIN4
    nsv4851470copy number variation1nstd200human GRCh37 chr17: 56,610,033-56,611,450 , GRCh38.p12 chr17: 58,532,672-58,534,089 SEPTIN4-AS1, SEPTIN4
    nsv4668097copy number variation1nstd186human GRCh37 chr17: 56,609,411-56,609,455 , GRCh38.p12 chr17: 58,532,050-58,532,094 SEPTIN4-AS1, SEPTIN4
    nsv4622820copy number variation1nstd183human GRCh37 chr17: 56,609,411-56,609,455 , GRCh38.p12 chr17: 58,532,050-58,532,094 SEPTIN4-AS1, SEPTIN4
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
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