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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057933inversion1nstd229human GRCh38 chr7: 63,377,139-65,038,693 , GRCh37.p13 chr7: 62,837,517-64,499,071 , VN1R36P, 91 more genes
    nsv7048702inversion1nstd229human GRCh38 chr7: 63,244,019-63,473,645 , GRCh37.p13 chr7: 62,704,397-62,934,023 LOC100287834, SLC25A1P2, 13 more genes
    nsv7042541inversion1nstd229human GRCh38 chr7: 63,218,809-63,459,253 , GRCh37.p13 chr7: 62,679,187-62,919,631 PHKG1P1, LOC101929050, 14 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
    nsv6632414copy number variation1nstd224human GRCh37 chr7: 62,360,358-62,935,337 , GRCh38.p12 chr7: 62,899,980-63,474,959 ZNF733P, ARAFP2, 20 more genes
    nsv6632413copy number variation1nstd224human GRCh37 chr7: 62,241,041-64,438,809 , GRCh38.p12 chr7: 62,780,663-64,978,431 , ZNF138, 99 more genes
    nsv6632349copy number variation1nstd224human GRCh37 chr7: 62,047,108-62,917,879 , GRCh38.p12 chr7: 62,586,730-63,457,501 LOC100287704, VN1R30P, 20 more genes
    nsv6631980copy number variation1nstd224human GRCh37 chr7: 62,113,011-62,917,879 , GRCh38.p12 chr7: 62,652,633-63,457,501 ZNF733P, ARAFP2, 20 more genes
    nsv6611054copy number variation1nstd223human GRCh38 chr7: 62,588,399-63,472,058 , GRCh37.p13 chr7: 62,048,777-62,932,436 ZNF90P3, LINC03075, 20 more genes
    nsv6567855inversion1nstd223human GRCh38 chr7: 63,220,242-63,522,939 , GRCh37.p13 chr7: 62,680,620-62,983,317 ARAFP2, ARAFP3, 16 more genes
    nsv6567601inversion1nstd223human GRCh38 chr7: 63,220,261-63,522,920 , GRCh37.p13 chr7: 62,680,639-62,983,298 VN1R33P, ARAFP2, 16 more genes
    nsv6565695inversion1nstd223human GRCh38 chr7: 63,290,325-63,457,746 , GRCh37.p13 chr7: 62,750,703-62,918,124 LOC100287704, ZNF734P, 12 more genes
    nsv6561751inversion1nstd223human GRCh38 chr7: 63,289,312-63,486,619 , GRCh37.p13 chr7: 62,749,690-62,946,997 VN1R31P, LOC102724738, 12 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6141582copy number variation1nstd206human GRCh38 chr7: 63,302,779-63,594,779 , GRCh37.p13 chr7: 62,763,157-63,055,157 , TNRC18P2, 18 more genes
    nsv6105327inversion1nstd212human GRCh38 chr7: 63,277,856-63,457,881 , GRCh37.p13 chr7: 62,738,234-62,918,259 , ARAFP3, 14 more genes
    nsv5976519inversion1nstd209human GRCh38 chr7: 63,374,409-63,521,610 , GRCh37.p13 chr7: 62,834,787-62,981,988 , ARAFP2, 9 more genes
    nsv5973368inversion1nstd209human GRCh38 chr7: 63,246,026-63,525,509 , GRCh37.p13 chr7: 62,706,404-62,985,887 , ARAFP3, 17 more genes
    nsv5669339inversion1nstd207human GRCh37.p13 chr7: 62,752,532-63,107,579 , GRCh38 chr7: 63,292,154-63,647,201 , TNRC18P2, 19 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
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