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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7043886inversion1nstd229human GRCh38 chr7: 25,072,526-28,462,757 , GRCh37.p13 chr7: 25,112,145-28,502,375 HOXA3, CREB5, 72 more genes
    nsv6817918copy number variation1nstd229human GRCh38 chr7: 26,620,103-26,620,180 , GRCh37.p13 chr7: 26,659,722-26,659,799 LOC101928077
    nsv6814153copy number variation1nstd229human GRCh38 chr7: 26,612,789-26,629,367 , GRCh37.p13 chr7: 26,652,408-26,668,986 LOC101928077
    nsv6813676copy number variation1nstd229human GRCh38 chr7: 26,616,256-26,616,622 , GRCh37.p13 chr7: 26,655,875-26,656,241 LOC101928077
    nsv6807062copy number variation1nstd229human GRCh38 chr7: 26,611,293-26,611,433 , GRCh37.p13 chr7: 26,650,912-26,651,052 LOC101928077
    nsv6800325copy number variation1nstd229human GRCh38 chr7: 26,491,289-26,605,760 , GRCh37.p13 chr7: 26,530,909-26,645,379 LINC02981, KIAA0087, 2 more genes
    nsv6636197copy number variation1nstd102humanUncertain significance GRCh37 chr7: 26,418,391-28,323,299 , GRCh38.p12 chr7: 26,378,771-28,283,680 LINC02860, LINC03095, 49 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
    nsv6608666copy number variation1nstd223human GRCh38 chr7: 26,612,789-26,629,365 , GRCh37.p13 chr7: 26,652,408-26,668,984 LOC101928077
    nsv6575237inversion1nstd223human GRCh38 chr7: 26,605,408-26,605,956 , GRCh37.p13 chr7: 26,645,027-26,645,575 LOC101928077
    nsv6562499inversion1nstd223human GRCh38 chr7: 25,072,527-28,462,755 , GRCh37.p13 chr7: 25,112,146-28,502,373 HOXA10-AS, HOXA2, 72 more genes
    nsv6315453copy number variation1nstd102humanPathogenic GRCh37 chr7: 25,451,740-33,864,069 , GRCh38.p12 chr7: 25,412,121-33,824,457 PLEKHA8, NFE2L3, 141 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313591copy number variation1nstd102humanUncertain significance GRCh37 chr7: 26,270,121-27,193,008 , GRCh38.p12 chr7: 26,230,501-27,153,389 HOXA1, RPL23P7, 22 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
    nsv6135989copy number variation1nstd213human GRCh37 chr7: 25,680,000-28,100,001 , GRCh38.p12 chr7: 25,640,380-28,060,382 HOXA2, HOXA5, 58 more genes
    nsv6135915copy number variation1nstd213human GRCh37 chr7: 26,520,000-27,320,001 , GRCh38.p12 chr7: 26,480,380-27,280,382 EVX1, HOXA1, 30 more genes
    nsv6071240insertion1nstd212human GRCh38 chr7: 26,606,191-26,606,191 , GRCh37.p13 chr7: 26,645,810-26,645,810 LOC101928077
    nsv5926697copy number variation1nstd209human GRCh38 chr7: 26,611,293-26,611,432 , GRCh37.p13 chr7: 26,650,912-26,651,051 LOC101928077
    nsv5919512copy number variation1nstd209human GRCh38 chr7: 26,509,679-33,120,288 , GRCh37.p13 chr7: 26,549,298-33,159,900 , CPVL-AS1, 126 more genes
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