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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097628copy number variation1nstd102humanUncertain significance GRCh37 chr7: 44,153,173-44,365,020 , GRCh38.p12 chr7: 44,113,574-44,325,421 LOC105375257, AEBP1, 7 more genes
    nsv7097375copy number variation1nstd102humanUncertain significance GRCh37 chr7: 43,810,758-44,747,598 , GRCh38.p12 chr7: 43,771,159-44,707,999 RASA4CP, OGDH, 31 more genes
    nsv6834700copy number variation1nstd229human GRCh38 chr7: 44,125,000-44,232,183 , GRCh37.p13 chr7: 44,164,599-44,271,782 CAMK2B, GCK, 5 more genes
    nsv6827874copy number variation1nstd229human GRCh38 chr7: 44,195,498-44,200,181 , GRCh37.p13 chr7: 44,235,097-44,239,780 YKT6
    nsv6824378copy number variation1nstd229human GRCh38 chr7: 43,852,301-44,460,500 , GRCh37.p13 chr7: 43,891,900-44,500,099 DBNL, GCK, 23 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
    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
    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
    nsv6136183copy number variation1nstd213human GRCh37 chr7: 43,240,000-44,280,001 , GRCh38.p12 chr7: 43,200,401-44,240,402 GCK, YKT6, 31 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
    nsv6135767copy number variation1nstd213human GRCh37 chr7: 44,150,000-44,300,001 , GRCh38.p12 chr7: 44,110,401-44,260,402 CAMK2B, GCK, 8 more genes
    nsv6011410copy number variation1nstd212human GRCh38 chr7: 44,200,567-44,200,655 , GRCh37.p13 chr7: 44,240,166-44,240,254 YKT6
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5483016copy number variation1nstd206human GRCh38 chr7: 44,211,125-44,212,246 , GRCh37.p13 chr7: 44,250,724-44,251,845 YKT6
    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
    nsv5378732translocation1nstd200human GRCh38 chr7: 44,206,061-44,206,061 , GRCh38 chr7: 44,205,990-44,205,990 , GRCh37.p13 chr7: 44,245,660-44,245,660 , GRCh37.p13 chr7: 44,245,589-44,245,589 YKT6
    nsv5333784translocation1nstd200human GRCh37 chr7: 44,245,660-44,245,660 , GRCh37 chr7: 44,245,589-44,245,589 , GRCh38.p12 chr7: 44,205,990-44,205,990 , GRCh38.p12 chr7: 44,206,061-44,206,061 YKT6
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