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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
    nsv7047140inversion1nstd229human GRCh38 chr5: 21,512,061-29,406,624 , GRCh37.p13 chr5: 21,512,170-29,406,731 AKTIPP2, RNU4-43P, 48 more genes
    nsv7042185inversion1nstd229human GRCh38 chr5: 29,141,180-29,144,605 , GRCh37.p13 chr5: 29,141,287-29,144,712 LINC02109, LOC105374699
    nsv7040926inversion1nstd229human GRCh38 chr5: 25,459,082-30,588,429 , GRCh37.p13 chr5: 25,459,191-30,588,536 LOC105374703, CCNB3P1, 32 more genes
    nsv6776976copy number variation1nstd229human GRCh38 chr5: 29,091,101-29,614,800 , GRCh37.p13 chr5: 29,091,208-29,614,907 LOC100420990, LOC100533677, 5 more genes
    nsv6771458copy number variation1nstd229human GRCh38 chr5: 29,164,656-29,202,850 , GRCh37.p13 chr5: 29,164,763-29,202,957 LINC02109
    nsv6769699copy number variation1nstd229human GRCh38 chr5: 29,072,356-29,871,727 , GRCh37.p13 chr5: 29,072,463-29,871,834 LINC02064, LOC105374703, 8 more genes
    nsv6768607copy number variation1nstd229human GRCh38 chr5: 28,626,079-29,191,397 , GRCh37.p13 chr5: 28,626,186-29,191,504 SUCLG2P4, LOC101929645, 5 more genes
    nsv6764106copy number variation1nstd229human GRCh38 chr5: 29,160,601-29,319,100 , GRCh37.p13 chr5: 29,160,708-29,319,207 LINC02109
    nsv6763508copy number variation1nstd229human GRCh38 chr5: 29,149,201-29,225,900 , GRCh37.p13 chr5: 29,149,308-29,226,007 LINC02109
    nsv6763412copy number variation1nstd229human GRCh38 chr5: 28,834,826-30,760,481 , GRCh37.p13 chr5: 28,834,933-30,760,588 LSP1P3, LINC02064, 18 more genes
    nsv6761600copy number variation1nstd229human GRCh38 chr5: 28,932,898-29,148,637 , GRCh37.p13 chr5: 28,933,005-29,148,744 SUCLG2P4, LOC101929645, 3 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 BASP1, RNU1-76P, 338 more genes
    nsv6630394copy number variation1nstd224human GRCh37 chr5: 28,942,952-29,143,203 , GRCh38.p12 chr5: 28,942,845-29,143,096 , GRCh38.p12 chr5|NW_003571036.1: 1-115,479 LOC101929645, LINC02109, 3 more genes
    nsv6567472inversion1nstd223human GRCh38 chr5: 29,167,408-29,168,083 , GRCh37.p13 chr5: 29,167,515-29,168,190 LINC02109
    nsv6388718copy number variation1nstd223human GRCh38 chr5: 29,141,401-29,142,600 , GRCh37.p13 chr5: 29,141,508-29,142,707 LOC105374699, LINC02109
    nsv6385784copy number variation1nstd223human GRCh38 chr5: 28,932,898-29,148,630 , GRCh37.p13 chr5: 28,933,005-29,148,737 LOC100533677, SUCLG2P4, 3 more genes
    nsv6315441copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-29,310,520 , GRCh38.p12 chr5: 113,461-29,310,413 FBXL7, LOC105374608, 319 more genes
    nsv6315416copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269 LOC105374649, LINC02196, 333 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
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