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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097363copy number variation2nstd102humanPathogenic GRCh37 chr7: 20,994,491-23,030,730 , GRCh38.p12 chr7: 20,954,872-22,991,111 STEAP1B-AS1, RNA5SP227, 25 more genes
    nsv7041207inversion1nstd229human GRCh38 chr7: 20,746,775-22,016,045 , GRCh37.p13 chr7: 20,786,398-22,055,663 LINC01162, RPL23P8, 12 more genes
    nsv6817040copy number variation1nstd229human GRCh38 chr7: 21,364,497-21,551,600 , GRCh37.p13 chr7: 21,404,115-21,591,218 MIR1183, RNU1-15P, 2 more genes
    nsv6811419copy number variation1nstd229human GRCh38 chr7: 21,462,371-21,474,212 , GRCh37.p13 chr7: 21,501,989-21,513,830 SP4, MIR1183
    nsv6807789copy number variation1nstd229human GRCh38 chr7: 21,471,219-21,475,398 , GRCh37.p13 chr7: 21,510,837-21,515,016 MIR1183, SP4
    nsv6801665copy number variation1nstd229human GRCh38 chr7: 21,018,519-21,566,612 , GRCh37.p13 chr7: 21,058,138-21,606,230 RN7SL542P, SP4, 6 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
    nsv6632062copy number variation1nstd224human GRCh37 chr7: 21,450,943-21,534,637 , GRCh38.p12 chr7: 21,411,325-21,495,019 MIR1183, SP4
    nsv6618825copy number variation1nstd223human GRCh38 chr7: 21,471,219-21,475,393 , GRCh37.p13 chr7: 21,510,837-21,515,011 SP4, MIR1183
    nsv6607273copy number variation1nstd223human GRCh38 chr7: 21,469,237-21,470,056 , GRCh37.p13 chr7: 21,508,855-21,509,674 SP4, MIR1183
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 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
    nsv6312441copy number variation1nstd102humanUncertain significance GRCh37 chr7: 20,994,491-23,213,917 , GRCh38.p12 chr7: 20,954,872-23,174,298 IL6, LOC105375186, 30 more genes
    nsv6136985copy number variation1nstd213human GRCh37 chr7: 20,170,000-22,450,001 , GRCh38.p12 chr7: 20,130,377-22,410,382 DNAH11, RAPGEF5, 23 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
    nsv5111264mobile element insertion1nstd203human GRCh38 chr7: 21,469,876-21,469,890 , GRCh37.p13 chr7: 21,509,494-21,509,508 MIR1183, SP4
    nsv4953472copy number variation1nstd200human GRCh38 chr7: 21,438,278-21,566,788 , GRCh37.p13 chr7: 21,477,896-21,606,406 SP4, DNAH11, 2 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4679554copy number variation1nstd189human GRCh37.p13 chr7: 21,462,825-21,776,281 , GRCh38.p12 chr7: 21,423,207-21,736,663 SP4, DNAH11, 2 more genes
    nsv4675166copy number variation1nstd102humanUncertain significance GRCh37 chr7: 21,483,799-21,542,891 , GRCh38.p12 chr7: 21,444,181-21,503,273 SP4, MIR1183
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