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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045327inversion1nstd229human GRCh38 chr7: 34,817,999-37,653,204 , GRCh37.p13 chr7: 34,857,611-37,692,807 ELMO1-AS1, DPY19L2P1, 40 more genes
    nsv7044771inversion1nstd229human GRCh38 chr7: 34,609,067-35,099,623 , GRCh37.p13 chr7: 34,648,679-35,139,235 NPSR1-AS1, DPY19L2P1, 8 more genes
    nsv6824166copy number variation1nstd229human GRCh38 chr7: 34,097,336-35,381,641 , GRCh37.p13 chr7: 34,136,948-35,421,251 LOC401324, NPSR1, 13 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6559554inversion1nstd223human GRCh38 chr7: 34,818,072-37,653,201 , GRCh37.p13 chr7: 34,857,684-37,692,804 LOC105375233, LOC107986734, 40 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313670copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 27,507,832-39,072,473 , GRCh38.p12 chr7: 27,468,213-39,032,873 ADCYAP1R1, AMPH, 175 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
    nsv6136990copy number variation1nstd213human GRCh37 chr7: 34,800,000-36,730,001 , GRCh38.p12 chr7: 34,760,388-36,690,396 EEPD1, NPSR1, 31 more genes
    nsv5975022inversion1nstd209human GRCh38 chr7: 34,818,028-37,653,165 , GRCh37.p13 chr7: 34,857,640-37,692,768 , AOAH, 41 more genes
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 more genes
    nsv5640439insertion1nstd207human GRCh38 chr7: 34,939,527-34,939,527 , GRCh37.p13 chr7: 34,979,139-34,979,139 DPY19L1, MIR548N, 1 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4769379copy number variation1nstd102humanUncertain significance GRCh37 chr7: 34,937,625-35,241,685 , GRCh38.p12 chr7: 34,898,013-35,202,073 DPY19L1, MIR548N, 5 more genes
    nsv4675405copy number variation1nstd102humanUncertain significance GRCh37 chr7: 34,432,783-35,083,191 , GRCh38.p12 chr7: 34,393,171-35,043,579 MIR548N, LOC105375228, 7 more genes
    nsv4675010copy number variation1nstd102humanUncertain significance GRCh37 chr7: 34,859,227-35,374,178 , GRCh38.p12 chr7: 34,819,615-35,334,568 LOC102724723, MIR548N, 8 more genes
    nsv4554420insertion1nstd166human GRCh37.p13 chr7: 34,978,804-34,978,804 , GRCh38.p12 chr7: 34,939,192-34,939,192 DPY19L1, MIR548N, 1 more genes
    nsv4525345copy number variation1nstd166human GRCh37.p13 chr7: 34,947,999-35,133,000 , GRCh38.p12 chr7: 34,908,387-35,093,388 MIR548N, DPY19L1, 3 more genes
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