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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048829inversion1nstd229human GRCh38 chr4: 118,673,463-118,679,105 , GRCh37.p13 chr4: 119,594,618-119,600,260 METTL14-DT
    nsv7043432inversion1nstd229human GRCh38 chr4: 117,041,189-125,064,058 , GRCh37.p13 chr4: 117,962,345-125,985,213 SEPTIN14P4, LINC02516, 109 more genes
    nsv6745399copy number variation1nstd229human GRCh38 chr4: 118,678,058-118,680,323 , GRCh37.p13 chr4: 119,599,213-119,601,478 METTL14-DT
    nsv6739389copy number variation1nstd229human GRCh38 chr4: 118,584,170-118,669,695 , GRCh37.p13 chr4: 119,505,325-119,590,850 CICP16, RNU6-1054P, 3 more genes
    nsv6738392copy number variation1nstd229human GRCh38 chr4: 118,579,485-118,673,752 , GRCh37.p13 chr4: 119,500,640-119,594,907 CICP16, SEPTIN14P4, 3 more genes
    nsv6570561inversion1nstd223human GRCh38 chr4: 117,041,188-125,064,052 , GRCh37.p13 chr4: 117,962,344-125,985,207 MYOZ2, NT5C3AP1, 109 more genes
    nsv6568953inversion1nstd223human GRCh38 chr4: 118,673,165-118,673,294 , GRCh37.p13 chr4: 119,594,320-119,594,449 METTL14-DT
    nsv6564355inversion1nstd223human GRCh38 chr4: 118,677,440-118,678,303 , GRCh37.p13 chr4: 119,598,595-119,599,458 METTL14-DT
    nsv6387569copy number variation1nstd223human GRCh38 chr4: 118,673,104-118,674,128 , GRCh37.p13 chr4: 119,594,259-119,595,283 METTL14-DT
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6313750copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,888,785-129,649,979 , GRCh38.p12 chr4: 115,967,629-128,728,824 LOC105377395, SEPTIN7P14, 152 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6290265copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113 LOC105379404, IL21-AS1, 218 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134734copy number variation1nstd213human GRCh37 chr4: 119,230,000-119,880,001 , GRCh38.p12 chr4: 118,308,845-118,958,846 PRSS12, SEC24D, 11 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv5995066copy number variation1nstd212human GRCh38 chr4: 118,673,188-118,673,927 , GRCh37.p13 chr4: 119,594,343-119,595,082 METTL14-DT
    nsv5570299copy number variation1nstd207human GRCh38 chr4: 118,671,407-118,671,747 , GRCh37.p13 chr4: 119,592,562-119,592,902 METTL14-DT
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5545494insertion1nstd206human GRCh38 chr4: 118,681,414-118,681,452 , GRCh37.p13 chr4: 119,602,569-119,602,607 METTL14-DT
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