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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057970inversion1nstd229human GRCh38 chr5: 39,369,727-42,623,585 , GRCh37.p13 chr5: 39,369,829-42,623,687 LINC02996, DAB2, 36 more genes
    nsv7057876inversion1nstd229human GRCh38 chr5: 40,785,368-40,874,865 , GRCh37.p13 chr5: 40,785,470-40,874,967 RPL37, SNORD72, 2 more genes
    nsv7041157inversion1nstd229human GRCh38 chr5: 40,200,630-42,327,400 , GRCh37.p13 chr5: 40,200,732-42,327,502 RNU7-161P, LINC02996, 26 more genes
    nsv6777504copy number variation1nstd229human GRCh38 chr5: 40,715,401-40,932,800 , GRCh37.p13 chr5: 40,715,503-40,932,902 RNU7-161P, RPL37, 6 more genes
    nsv6770506copy number variation1nstd229human GRCh38 chr5: 40,768,082-40,768,205 , GRCh37.p13 chr5: 40,768,184-40,768,307 PRKAA1
    nsv6769814copy number variation1nstd229human GRCh38 chr5: 39,447,462-42,528,554 , GRCh37.p13 chr5: 39,447,564-42,528,656 RNU7-161P, OXCT1, 35 more genes
    nsv6768943copy number variation1nstd229human GRCh38 chr5: 40,583,586-41,276,040 , GRCh37.p13 chr5: 40,583,688-41,276,142 TTC33, RPL37, 10 more genes
    nsv6768838copy number variation1nstd229human GRCh38 chr5: 40,794,513-40,794,876 , GRCh37.p13 chr5: 40,794,615-40,794,978 PRKAA1
    nsv6766958copy number variation1nstd229human GRCh38 chr5: 40,779,201-40,786,700 , GRCh37.p13 chr5: 40,779,303-40,786,802 PRKAA1
    nsv6763460copy number variation1nstd229human GRCh38 chr5: 39,215,959-40,973,214 , GRCh37.p13 chr5: 39,216,061-40,973,316 PRKAA1, PTGER4, 18 more genes
    nsv6761216copy number variation1nstd229human GRCh38 chr5: 40,785,401-40,859,200 , GRCh37.p13 chr5: 40,785,503-40,859,302 RPL37, CARD6, 2 more genes
    nsv6759529copy number variation1nstd229human GRCh38 chr5: 40,778,801-40,786,600 , GRCh37.p13 chr5: 40,778,903-40,786,702 PRKAA1
    nsv6758844copy number variation1nstd229human GRCh38 chr5: 40,772,757-40,772,955 , GRCh37.p13 chr5: 40,772,859-40,773,057 PRKAA1
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6560285inversion1nstd223human GRCh38 chr5: 40,770,365-40,770,709 , GRCh37.p13 chr5: 40,770,467-40,770,811 PRKAA1
    nsv6395194copy number variation1nstd223human GRCh38 chr5: 40,778,801-40,786,700 , GRCh37.p13 chr5: 40,778,903-40,786,802 PRKAA1
    nsv6389296copy number variation1nstd223human GRCh38 chr5: 40,765,301-40,766,400 , GRCh37.p13 chr5: 40,765,403-40,766,502 PRKAA1
    nsv6388865copy number variation1nstd223human GRCh38 chr5: 40,783,956-40,784,456 , GRCh37.p13 chr5: 40,784,058-40,784,558 PRKAA1
    nsv6388671copy number variation1nstd223human GRCh38 chr5: 39,447,462-42,528,554 , GRCh37.p13 chr5: 39,447,564-42,528,656 SERBP1P6, TCP1P2, 35 more genes
    nsv6387013copy number variation1nstd223human GRCh38 chr5: 40,794,513-40,794,876 , GRCh37.p13 chr5: 40,794,615-40,794,978 PRKAA1
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