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Items: 1 to 20 of 175

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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
    nsv7051859inversion1nstd229human GRCh38 chr5: 41,806,643-42,640,726 , GRCh37.p13 chr5: 41,806,745-42,640,828 RPS2P22, SERBP1P6, 11 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
    nsv6772752copy number variation1nstd229human GRCh38 chr5: 41,871,542-42,048,800 , GRCh37.p13 chr5: 41,871,644-42,048,902 RPS2P22, LOC102723752, 6 more genes
    nsv6771615copy number variation1nstd229human GRCh38 chr5: 41,879,700-42,913,283 , GRCh37.p13 chr5: 41,879,802-42,913,385 LOC100419715, PRELID3BP5, 14 more genes
    nsv6770863copy number variation1nstd229human GRCh38 chr5: 41,919,781-42,487,753 , GRCh37.p13 chr5: 41,919,883-42,487,855 RIMOC1, FBXO4, 7 more genes
    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
    nsv6764820copy number variation1nstd229human GRCh38 chr5: 41,901,820-41,903,615 , GRCh37.p13 chr5: 41,901,922-41,903,717 RIMOC1
    nsv6758494copy number variation1nstd229human GRCh38 chr5: 41,902,999-41,903,527 , GRCh37.p13 chr5: 41,903,101-41,903,629 RIMOC1
    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
    nsv6634390copy number variation1nstd102humanPathogenic GRCh37 chr5: 41,879,852-42,906,725 , GRCh38.p12 chr5: 41,879,750-42,906,623 PRELID3BP5, LOC100419715, 14 more genes
    nsv6634341copy number variation1nstd102humanPathogenic GRCh37 chr5: 41,879,852-42,913,979 , GRCh38.p12 chr5: 41,879,750-42,913,877 PPIAP77, LINC02996, 14 more genes
    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
    nsv6377152copy number variation1nstd223human GRCh38 chr5: 41,901,819-41,903,614 , GRCh37.p13 chr5: 41,901,921-41,903,716 RIMOC1
    nsv6377020copy number variation1nstd223human GRCh38 chr5: 41,903,001-41,903,600 , GRCh37.p13 chr5: 41,903,103-41,903,702 RIMOC1
    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
    nsv6136117copy number variation1nstd213human GRCh37 chr5: 41,590,000-44,160,001 , GRCh38.p12 chr5: 41,589,898-44,159,899 GHR, OXCT1, 44 more genes
    nsv6135410copy number variation1nstd213human GRCh37 chr5: 38,040,000-43,250,001 , GRCh38.p12 chr5: 38,039,898-43,249,899 FYB1, PTGER4, 78 more genes
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