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Items: 1 to 20 of 83

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056404inversion1nstd229human GRCh38 chr7: 45,643,008-53,582,757 , GRCh37.p13 chr7: 45,682,607-53,650,450 PKD1L1, FIGNL1, 79 more genes
    nsv7046943inversion1nstd229human GRCh38 chr7: 45,642,996-53,582,758 , GRCh37.p13 chr7: 45,682,595-53,650,451 CDC14C, ROBO2P1, 79 more genes
    nsv6831722copy number variation1nstd229human GRCh38 chr7: 45,885,822-45,888,259 , GRCh37.p13 chr7: 45,925,421-45,927,858 IGFBP1
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6617508copy number variation1nstd223human GRCh38 chr7: 45,885,822-45,888,254 , GRCh37.p13 chr7: 45,925,421-45,927,853 IGFBP1
    nsv6572893inversion1nstd223human GRCh38 chr7: 45,642,996-53,582,758 , GRCh37.p13 chr7: 45,682,595-53,650,451 LOC730234, LOC105375278, 79 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313509copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060 LINC01447, ABCA13, 142 more genes
    nsv6136999copy number variation1nstd213human GRCh37 chr7: 45,450,000-46,600,001 , GRCh38.p12 chr7: 45,410,401-46,560,403 TTC4P1, CICP20, 17 more genes
    nsv6136995copy number variation1nstd213human GRCh37 chr7: 39,040,000-48,190,001 , GRCh38.p12 chr7: 39,000,400-48,150,404 ADCY1, AEBP1, 161 more genes
    nsv6135992copy number variation1nstd213human GRCh37 chr7: 39,290,000-48,200,001 , GRCh38.p12 chr7: 39,250,401-48,160,404 PSMA2, RALA, 160 more genes
    nsv5914158copy number variation1nstd209human GRCh38 chr7: 45,885,818-45,888,253 , GRCh37.p13 chr7: 45,925,417-45,927,852 IGFBP1
    nsv5846626copy number variation1nstd209human GRCh38 chr7: 45,885,731-45,888,305 , GRCh37.p13 chr7: 45,925,330-45,927,904 IGFBP1
    nsv5556950sequence alteration1nstd206human GRCh38 chr7: 44,712,903-47,388,095 , GRCh37.p13 chr7: 44,752,502-47,427,692 , ADCY1, 51 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
    nsv5381787copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027 OGDH, LOC112267918, 110 more genes
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956486copy number variation1nstd200human GRCh38 chr7: 45,885,822-45,888,254 , GRCh37.p13 chr7: 45,925,421-45,927,853 IGFBP1
    nsv4811545copy number variation1nstd200human GRCh37 chr7: 45,925,421-45,927,853 , GRCh38.p12 chr7: 45,885,822-45,888,254 IGFBP1
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