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Items: 1 to 20 of 137

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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
    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
    nsv6773402copy number variation1nstd229human GRCh38 chr5: 29,035,227-29,134,538 , GRCh37.p13 chr5: 29,035,334-29,134,645 LOC100533677, LOC105374699, 1 more genes
    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
    nsv6765893copy number variation1nstd229human GRCh38 chr5: 28,791,192-29,128,300 , GRCh37.p13 chr5: 28,791,299-29,128,407 LSP1P3, LOC101929645, 3 more genes
    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
    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
    nsv6300383copy number variation1nstd186human GRCh37 chr5: 26,834,087-43,674,516 , GRCh38.p12 chr5: 26,833,978-43,674,414 , TMEM267, 221 more genes
    nsv6135173copy number variation1nstd213human GRCh37 chr5: 28,830,000-29,210,001 , GRCh38.p12 chr5: 28,829,893-29,209,894 LSP1P3, SUCLG2P4, 4 more genes
    nsv6135147copy number variation1nstd213human GRCh37 chr5: 28,130,000-30,010,001 , GRCh38.p12 chr5: 28,129,893-30,009,894 PGBD3P2, LSP1P3, 20 more genes
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
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