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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7045933inversion1nstd229human GRCh38 chr5: 9,205,469-10,383,964 , GRCh37.p13 chr5: 9,205,581-10,384,076 SEMA5A-AS1, SNORD123, 15 more genes
    nsv6777555copy number variation1nstd229human GRCh38 chr5: 9,487,161-9,509,531 , GRCh37.p13 chr5: 9,487,273-9,509,643 SEMA5A, SEMA5A-AS1
    nsv6773219copy number variation1nstd229human GRCh38 chr5: 7,865,454-9,761,641 , GRCh37.p13 chr5: 7,865,567-9,761,753 TAS2R1, LINC02226, 22 more genes
    nsv6773005copy number variation1nstd229human GRCh38 chr5: 9,516,463-9,516,493 , GRCh37.p13 chr5: 9,516,575-9,516,605 SEMA5A-AS1, SEMA5A
    nsv6769188copy number variation1nstd229human GRCh38 chr5: 9,225,010-9,603,728 , GRCh37.p13 chr5: 9,225,122-9,603,840 SNHG18, SEMA5A, 3 more genes
    nsv6766634copy number variation1nstd229human GRCh38 chr5: 9,181,906-9,845,112 , GRCh37.p13 chr5: 9,182,018-9,845,224 SNHG18, SEMA5A-AS1, 7 more genes
    nsv6764486copy number variation1nstd229human GRCh38 chr5: 9,477,059-10,373,440 , GRCh37.p13 chr5: 9,477,171-10,373,552 LOC107986405, MARCHF6-DT, 15 more genes
    nsv6762398copy number variation1nstd229human GRCh38 chr5: 9,517,697-9,518,286 , GRCh37.p13 chr5: 9,517,809-9,518,398 SEMA5A-AS1, SEMA5A
    nsv6637149copy number variation1nstd102humanPathogenic GRCh37 chr5: 8,081,005-22,210,970 , GRCh38.p12 chr5: 8,080,892-22,210,861 LOC107986376, MARCHF11, 150 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636849copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-17,654,787 , GRCh38.p12 chr5: 113,462-17,654,678 ADCY2, HMGB3P3, 248 more genes
    nsv6636672copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743 LINC02123, LINC01020, 302 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
    nsv6391357copy number variation1nstd223human GRCh38 chr5: 9,515,401-9,515,992 , GRCh37.p13 chr5: 9,515,513-9,516,104 SEMA5A, SEMA5A-AS1
    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
    nsv6315334copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-12,601,027 , GRCh38.p12 chr5: 113,461-12,600,915 LOC105374642, LOC107986395, 173 more genes
    nsv6291304copy number variation1nstd102humanLikely benign GRCh37 chr5: 9,074,626-10,073,956 , GRCh38.p12 chr5: 9,074,514-10,073,844 SEMA5A-AS1, TAS2R1, 9 more genes
    nsv6291096copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-16,952,167 , GRCh38.p12 chr5: 113,462-16,952,058 MIR4457, HNRNPKP5, 222 more genes
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