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Items: 1 to 20 of 132

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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
    nsv7046164inversion1nstd229human GRCh38 chr5: 36,152,155-36,160,427 , GRCh37.p13 chr5: 36,152,257-36,160,529 LMBRD2, SKP2, 1 more genes
    nsv7038792inversion1nstd229human GRCh38 chr5: 36,155,778-36,160,064 , GRCh37.p13 chr5: 36,155,880-36,160,166 SKP2
    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
    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
    nsv6572148inversion1nstd223human GRCh38 chr5: 33,560,391-36,411,977 , GRCh37.p13 chr5: 33,560,496-36,412,079 C1QTNF3, RAI14-DT, 36 more genes
    nsv6557194inversion1nstd223human GRCh38 chr5: 36,167,622-36,169,452 , GRCh37.p13 chr5: 36,167,724-36,169,554 SKP2
    nsv6395123copy number variation1nstd223human GRCh38 chr5: 36,179,001-36,179,800 , GRCh37.p13 chr5: 36,179,103-36,179,902 SKP2
    nsv6377525copy number variation1nstd223human GRCh38 chr5: 36,160,237-36,160,865 , GRCh37.p13 chr5: 36,160,339-36,160,967 SKP2
    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
    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
    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
    nsv5473575copy number variation1nstd206human GRCh38 chr5: 36,172,019-36,176,092 , GRCh37.p13 chr5: 36,172,121-36,176,194 SKP2
    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
    nsv5083224mobile element insertion1nstd203human GRCh38 chr5: 36,183,953-36,183,969 , GRCh37.p13 chr5: 36,184,055-36,184,071 SKP2
    nsv4569390sequence alteration1nstd166human GRCh37.p13 chr5: 36,152,256-36,160,529 , GRCh38.p12 chr5: 36,152,154-36,160,427 SKP2, LMBRD2, 1 more genes
    nsv4547364insertion1nstd166human GRCh37.p13 chr5: 36,184,343-36,184,343 , GRCh38.p12 chr5: 36,184,241-36,184,241 SKP2
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