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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7074105inversion1nstd229human GRCh38 chr10: 17,945,641-22,801,235 , GRCh37.p13 chr10: 18,252,931-23,090,164 UBE2V2P1, LOC105376450, 62 more genes
    nsv6893333copy number variation1nstd229human GRCh38 chr10: 20,964,833-22,078,565 , GRCh37.p13 chr10: 21,253,762-22,367,494 RN7SKP219, RN7SKP37, 19 more genes
    nsv6891034copy number variation1nstd229human GRCh38 chr10: 19,515,837-21,850,350 , GRCh37.p13 chr10: 19,804,766-22,139,279 LOC107984214, LOC101928834, 31 more genes
    nsv6888356copy number variation1nstd229human GRCh38 chr10: 21,513,811-21,518,059 , GRCh37.p13 chr10: 21,802,740-21,806,988 SKIDA1
    nsv6878997copy number variation1nstd229human GRCh38 chr10: 21,497,501-21,535,500 , GRCh37.p13 chr10: 21,786,430-21,824,429 SKIDA1, MLLT10, 1 more genes
    nsv6591556inversion1nstd223human GRCh38 chr10: 21,101,301-21,842,530 , GRCh37.p13 chr10: 21,390,230-22,131,459 LOC100420467, LOC107984214, 17 more genes
    nsv6447831copy number variation1nstd223human GRCh38 chr10: 21,508,401-21,510,500 , GRCh37.p13 chr10: 21,797,330-21,799,429 SKIDA1
    nsv6446991copy number variation1nstd223human GRCh38 chr10: 21,525,801-21,527,600 , GRCh37.p13 chr10: 21,814,730-21,816,529 SKIDA1, MLLT10
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6132032copy number variation1nstd213human GRCh37 chr10: 21,540,000-22,750,001 , GRCh38.p12 chr10: 21,251,071-22,461,072 BMI1, MLLT10, 29 more genes
    nsv6132031copy number variation1nstd213human GRCh37 chr10: 18,100,000-28,260,001 , GRCh38.p12 chr10: 17,839,748-27,971,072 BMI1, CACNB2, 136 more genes
    nsv4455084copy number variation1nstd102humanUncertain significance GRCh37 chr10: 19,774,176-22,330,966 , GRCh38.p12 chr10: 19,485,247-22,042,037 LOC105376445, NEBL-AS1, 33 more genes
    nsv4423754copy number variation1nstd174human GRCh37 chr10: 21,762,506-21,845,875 , GRCh38.p12 chr10: 21,473,577-21,556,946 SKIDA1, MIR1915HG, 2 more genes
    nsv4389293copy number variation1nstd171human GRCh37 chr10: 21,805,799-21,806,056 , GRCh38.p12 chr10: 21,516,870-21,517,127 SKIDA1
    nsv4389282copy number variation1nstd171human GRCh37 chr10: 21,805,799-21,806,032 , GRCh38.p12 chr10: 21,516,870-21,517,103 SKIDA1
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 more genes
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