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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052690inversion1nstd229human GRCh38 chr7: 42,600,188-42,792,852 , GRCh37.p13 chr7: 42,639,787-42,832,451 TCP1P1, LINC01448
    nsv7047375inversion1nstd229human GRCh38 chr7: 42,695,428-42,695,528 , GRCh37.p13 chr7: 42,735,027-42,735,127 LINC01448
    nsv6826787copy number variation1nstd229human GRCh38 chr7: 42,376,110-43,620,614 , GRCh37.p13 chr7: 42,415,709-43,660,213 LUARIS, PSMA2, 19 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
    nsv6611115copy number variation1nstd223human GRCh38 chr7: 42,664,356-42,664,849 , GRCh37.p13 chr7: 42,703,955-42,704,448 LINC01448
    nsv6605472copy number variation1nstd223human GRCh38 chr7: 42,667,334-42,667,904 , GRCh37.p13 chr7: 42,706,933-42,707,503 LINC01448
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 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
    nsv6307729mobile element insertion1nstd186human GRCh37 chr7: 42,740,639-42,740,690 , GRCh38.p12 chr7: 42,701,040-42,701,091 LINC01448
    nsv6304849copy number variation1nstd186human GRCh37 chr7: 42,701,596-42,701,710 , GRCh38.p12 chr7: 42,661,997-42,662,111 LINC01448
    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
    nsv5909610copy number variation1nstd209human GRCh38 chr7: 42,689,745-42,689,851 , GRCh37.p13 chr7: 42,729,344-42,729,450 LINC01448
    nsv5725809mobile element insertion1nstd211human GRCh38 chr7: 42,701,040-42,701,040 , GRCh37.p13 chr7: 42,740,639-42,740,639 LINC01448
    nsv5719915mobile element insertion1nstd211human GRCh38 chr7: 42,696,396-42,696,396 , GRCh37.p13 chr7: 42,735,995-42,735,995 LINC01448
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5555395mobile element insertion1nstd206human GRCh38 chr7: 42,701,040-42,701,091 , GRCh37.p13 chr7: 42,740,639-42,740,690 LINC01448
    nsv5493641copy number variation1nstd206human GRCh38 chr7: 42,661,997-42,662,111 , GRCh37.p13 chr7: 42,701,596-42,701,710 LINC01448
    nsv5493059copy number variation1nstd206human GRCh38 chr7: 42,689,747-42,689,852 , GRCh37.p13 chr7: 42,729,346-42,729,451 LINC01448
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