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Items: 1 to 20 of 448

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053681inversion1nstd229human GRCh38 chr4: 77,521,084-77,890,370 , GRCh37.p13 chr4: 78,442,238-78,811,524 MRPL1, LOC105377296, 3 more genes
    nsv7049185inversion1nstd229human GRCh38 chr4: 77,808,799-83,184,403 , GRCh37.p13 chr4: 78,729,953-84,105,556 VAMP9P, HNRNPA3P13, 75 more genes
    nsv7042194inversion1nstd229human GRCh38 chr4: 77,723,620-77,730,437 , GRCh37.p13 chr4: 78,644,774-78,651,591 CNOT6L
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv7039784inversion1nstd229human GRCh38 chr4: 77,707,518-77,713,077 , GRCh37.p13 chr4: 78,628,672-78,634,231 CNOT6L
    nsv6757688copy number variation1nstd229human GRCh38 chr4: 77,798,873-77,803,795 , GRCh37.p13 chr4: 78,720,027-78,724,949 CNOT6L
    nsv6751275copy number variation1nstd229human GRCh38 chr4: 77,745,277-77,748,254 , GRCh37.p13 chr4: 78,666,431-78,669,408 CNOT6L
    nsv6750735copy number variation1nstd229human GRCh38 chr4: 77,804,900-77,819,466 , GRCh37.p13 chr4: 78,726,054-78,740,620 CNOT6L
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6746141copy number variation1nstd229human GRCh38 chr4: 77,801,333-77,802,030 , GRCh37.p13 chr4: 78,722,487-78,723,184 CNOT6L
    nsv6745233copy number variation1nstd229human GRCh38 chr4: 77,778,201-77,808,700 , GRCh37.p13 chr4: 78,699,355-78,729,854 CNOT6L
    nsv6743722copy number variation1nstd229human GRCh38 chr4: 77,804,614-77,804,710 , GRCh37.p13 chr4: 78,725,768-78,725,864 CNOT6L
    nsv6742866copy number variation1nstd229human GRCh38 chr4: 77,804,844-77,809,080 , GRCh37.p13 chr4: 78,725,998-78,730,234 CNOT6L
    nsv6740227copy number variation1nstd229human GRCh38 chr4: 77,713,217-77,713,321 , GRCh37.p13 chr4: 78,634,371-78,634,475 CNOT6L
    nsv6739071copy number variation1nstd229human GRCh38 chr4: 77,724,741-77,724,812 , GRCh37.p13 chr4: 78,645,895-78,645,966 CNOT6L
    nsv6637002copy number variation1nstd102humanUncertain significance GRCh37 chr4: 78,117,589-78,749,042 , GRCh38.p12 chr4: 77,196,436-77,827,888 CXCL13, LOC100421141, 6 more genes
    nsv6629987copy number variation1nstd224human GRCh37 chr4: 78,006,206-78,834,532 , GRCh38.p12 chr4: 77,085,053-77,913,378 MRPL1, LOC339966, 12 more genes
    nsv6629735copy number variation1nstd224human GRCh37 chr4: 76,885,365-79,465,559 , GRCh38.p12 chr4: 75,964,212-78,544,405 CCNI, NUP54, 54 more genes
    nsv6565964inversion1nstd223human GRCh38 chr4: 77,257,732-78,114,933 , GRCh37.p13 chr4: 78,178,885-79,036,087 LOC102724916, CNOT6L, 12 more genes
    nsv6565136inversion1nstd223human GRCh38 chr4: 74,413,523-83,001,891 , GRCh37.p13 chr4: 75,279,240-83,923,044 RNU6-615P, SHROOM3, 144 more genes
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