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Items: 1 to 20 of 93

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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
    nsv6828952copy number variation1nstd229human GRCh38 chr7: 42,797,063-42,797,112 , GRCh37.p13 chr7: 42,836,662-42,836,711 TCP1P1
    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
    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
    nsv6305128copy number variation1nstd186human GRCh37 chr7: 42,792,319-42,853,790 , GRCh38.p12 chr7: 42,752,720-42,814,191 TCP1P1
    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
    nsv6135766copy number variation1nstd213human GRCh37 chr7: 42,750,000-42,920,001 , GRCh38.p12 chr7: 42,710,401-42,880,402 TCP1P1, LOC107986735
    nsv5846981copy number variation1nstd209human GRCh38 chr7: 42,787,446-42,792,842 , GRCh37.p13 chr7: 42,827,045-42,832,441 TCP1P1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5488468copy number variation1nstd206human GRCh38 chr7: 42,752,720-42,814,191 , GRCh37.p13 chr7: 42,792,319-42,853,790 TCP1P1
    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
    nsv4953626copy number variation1nstd200human GRCh38 chr7: 42,376,110-43,620,617 , GRCh37.p13 chr7: 42,415,709-43,660,216 TCP1P1, LOC105375250, 19 more genes
    nsv4675195copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,397,582-42,870,176 , GRCh38.p12 chr7: 41,357,984-42,830,577 LOC105375247, LOC107986787, 11 more genes
    nsv4604338copy number variation1nstd183human GRCh37 chr7: 42,830,554-42,864,221 , GRCh38.p12 chr7: 42,790,955-42,824,622 TCP1P1
    nsv4456214copy number variation2nstd102humanUncertain significance GRCh37 chr7: 42,417,642-43,658,492 , GRCh38.p12 chr7: 42,378,043-43,618,893 RPL18AP10, LOC105375252, 19 more genes
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