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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097139copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-39,364,566 , GRCh38.p12 chr5: 33,944,648-39,364,464 RNU7-75P, UGT3A1, 77 more genes
    nsv7047572inversion1nstd229human GRCh38 chr5: 38,711,108-38,714,114 , GRCh37.p13 chr5: 38,711,210-38,714,216 OSMR-DT, LINC01265
    nsv6775050copy number variation1nstd229human GRCh38 chr5: 38,597,809-38,803,173 , GRCh37.p13 chr5: 38,597,911-38,803,275 LINC01265, LIFR-AS1, 4 more genes
    nsv6769429copy number variation1nstd229human GRCh38 chr5: 35,077,787-40,637,192 , GRCh37.p13 chr5: 35,077,889-40,637,294 LINC02110, LOC105374735, 68 more genes
    nsv6764301copy number variation1nstd229human GRCh38 chr5: 37,395,324-40,706,253 , GRCh37.p13 chr5: 37,395,426-40,706,355 DAB2, LOC107986414, 39 more genes
    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
    nsv6382601copy number variation1nstd223human GRCh38 chr5: 38,597,809-38,803,172 , GRCh37.p13 chr5: 38,597,911-38,803,274 OSMR-DT, LIFR-AS1, 4 more genes
    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
    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
    nsv6135409copy number variation1nstd213human GRCh37 chr5: 36,380,000-41,260,001 , GRCh38.p12 chr5: 36,379,898-41,259,899 PTGER4, TTC33, 64 more genes
    nsv6135175copy number variation1nstd213human GRCh37 chr5: 29,210,000-46,400,001 , GRCh38.p12 chr5: 29,209,893-46,399,899 CDH6, HMGCS1, 210 more genes
    nsv6135152copy number variation1nstd213human GRCh37 chr5: 38,620,000-43,420,001 , GRCh38.p12 chr5: 38,619,898-43,419,899 C6, C9, 70 more genes
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 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
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv4944622copy number variation1nstd200human GRCh38 chr5: 38,693,304-38,793,720 , GRCh37.p13 chr5: 38,693,406-38,793,822 LOC100132789, LINC01265, 2 more genes
    nsv4680426copy number variation1nstd189human GRCh37.p13 chr5: 37,623,394-42,403,769 , GRCh38.p12 chr5: 37,623,292-42,403,667 , C6, 65 more genes
    nsv4674231copy number variation1nstd102humanPathogenic GRCh37 chr5: 38,432,180-49,441,945 , GRCh38.p12 chr5: 38,432,078-50,146,111 RPSAP38, LOC105374746, 92 more genes

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