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Items: 1 to 20 of 195

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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
    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
    nsv6771068copy number variation1nstd229human GRCh38 chr5: 40,735,766-40,740,484 , GRCh37.p13 chr5: 40,735,868-40,740,586 TTC33, PTGER4
    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
    nsv6769635copy number variation1nstd229human GRCh38 chr5: 40,720,501-40,726,400 , GRCh37.p13 chr5: 40,720,603-40,726,502 PTGER4, TTC33
    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
    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
    nsv6763103copy number variation1nstd229human GRCh38 chr5: 40,748,942-40,753,587 , GRCh37.p13 chr5: 40,749,044-40,753,689 TTC33
    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
    nsv6562709inversion1nstd223human GRCh38 chr5: 40,748,060-40,748,947 , GRCh37.p13 chr5: 40,748,162-40,749,049 TTC33
    nsv6395261copy number variation1nstd223human GRCh38 chr5: 40,721,901-40,723,200 , GRCh37.p13 chr5: 40,722,003-40,723,302 TTC33, PTGER4
    nsv6392817copy number variation1nstd223human GRCh38 chr5: 40,747,891-40,748,262 , GRCh37.p13 chr5: 40,747,993-40,748,364 TTC33
    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
    nsv6385660copy number variation1nstd223human GRCh38 chr5: 40,716,401-40,722,400 , GRCh37.p13 chr5: 40,716,503-40,722,502 TTC33, PTGER4
    nsv6385051copy number variation1nstd223human GRCh38 chr5: 40,720,448-40,726,442 , GRCh37.p13 chr5: 40,720,550-40,726,544 PTGER4, TTC33
    nsv6377822copy number variation1nstd223human GRCh38 chr5: 40,735,766-40,740,480 , GRCh37.p13 chr5: 40,735,868-40,740,582 PTGER4, TTC33
    nsv6315368copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,053,583-46,389,339 , GRCh38.p12 chr5: 36,053,481-46,389,237 C7, RIMOC1, 128 more genes
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
    nsv6300383copy number variation1nstd186human GRCh37 chr5: 26,834,087-43,674,516 , GRCh38.p12 chr5: 26,833,978-43,674,414 , TMEM267, 221 more genes
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