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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057944inversion1nstd229human GRCh38 chr5: 172,134,356-176,589,266 , GRCh37.p13 chr5: 171,561,360-176,016,267 MIR10523, NIFKP2, 92 more genes
    nsv7057428inversion1nstd229human GRCh38 chr5: 173,607,624-173,607,638 , GRCh37.p13 chr5: 173,034,627-173,034,641 BOD1
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6789745copy number variation1nstd229human GRCh38 chr5: 173,610,079-173,610,679 , GRCh37.p13 chr5: 173,037,082-173,037,682 BOD1
    nsv6781511copy number variation1nstd229human GRCh38 chr5: 170,662,244-174,111,903 , GRCh37.p13 chr5: 170,089,248-173,538,906 LOC101928093, LOC107986482, 79 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6630496copy number variation1nstd224human GRCh37 chr5: 172,769,501-173,542,110 , GRCh38.p12 chr5: 173,342,498-174,115,107 LINC01485, LOC107986482, 15 more genes
    nsv6630075copy number variation1nstd224human GRCh37 chr5: 172,988,569-173,037,054 , GRCh38.p12 chr5: 173,561,566-173,610,051 LINC02995, BOD1
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135131copy number variation1nstd213human GRCh37 chr5: 172,850,000-173,410,001 , GRCh38.p12 chr5: 173,422,997-173,982,998 CPEB4, BOD1, 9 more genes
    nsv5902849copy number variation1nstd209human GRCh38 chr5: 173,608,292-173,609,236 , GRCh37.p13 chr5: 173,035,295-173,036,239 BOD1
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5896854copy number variation1nstd209human GRCh38 chr5: 173,609,432-173,613,127 , GRCh37.p13 chr5: 173,036,435-173,040,130 BOD1
    nsv5728773mobile element insertion1nstd211human GRCh38 chr5: 173,609,434-173,609,434 , GRCh37.p13 chr5: 173,036,437-173,036,437 BOD1
    nsv5724374mobile element insertion1nstd211human GRCh38 chr5: 173,608,133-173,608,133 , GRCh37.p13 chr5: 173,035,136-173,035,136 BOD1
    nsv5461467copy number variation1nstd206human GRCh38 chr5: 173,608,294-173,609,237 , GRCh37.p13 chr5: 173,035,297-173,036,240 BOD1
    nsv4949231copy number variation1nstd200human GRCh38 chr5: 173,571,609-173,858,663 , GRCh37.p13 chr5: 172,998,612-173,285,666 , BOD1, 7 more genes
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4763538inversion1nstd199human GRCh37 chr5: 170,260,689-178,183,120 , GRCh38.p12 chr5: 170,833,685-178,756,119 , BNIP1, 194 more genes
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