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Items: 1 to 20 of 97

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146831insertion1nstd232human GRCh37.p13 chr7: 44,620,839-44,620,839 , GRCh38.p12 chr7: 44,581,240-44,581,240 TMED4
    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
    nsv6831634copy number variation1nstd229human GRCh38 chr7: 44,578,685-44,581,256 , GRCh37.p13 chr7: 44,618,284-44,620,855 TMED4
    nsv6825179copy number variation1nstd229human GRCh38 chr7: 44,580,239-44,583,329 , GRCh37.p13 chr7: 44,619,838-44,622,928 TMED4
    nsv6820964copy number variation1nstd229human GRCh38 chr7: 44,572,747-44,579,131 , GRCh37.p13 chr7: 44,612,346-44,618,730 TMED4, DDX56
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6611289copy number variation1nstd223human GRCh38 chr7: 44,580,306-44,580,776 , GRCh37.p13 chr7: 44,619,905-44,620,375 TMED4
    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
    nsv6135995copy number variation1nstd213human GRCh37 chr7: 44,480,000-45,360,001 , GRCh38.p12 chr7: 44,440,401-45,320,402 PURB, NPC1L1, 28 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
    nsv5911634copy number variation1nstd209human GRCh38 chr7: 44,580,306-44,580,775 , GRCh37.p13 chr7: 44,619,905-44,620,374 TMED4
    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
    nsv5198734mobile element insertion1nstd203human GRCh38 chr7: 44,577,945-44,577,959 , GRCh37.p13 chr7: 44,617,544-44,617,558 TMED4
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4616910copy number variation1nstd183human GRCh37 chr7: 44,606,217-44,688,085 , GRCh38.p12 chr7: 44,566,618-44,648,486 OGDH, DDX56, 1 more genes
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