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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146913insertion1nstd232human GRCh37.p13 chr2: 42,580,486-42,580,486 , GRCh38.p12 chr2: 42,353,346-42,353,346 COX7A2L
    nsv7142953insertion1nstd232human GRCh37.p13 chr2: 42,578,506-42,578,506 , GRCh38.p12 chr2: 42,351,366-42,351,366 COX7A2L
    nsv7142390insertion1nstd232human GRCh37.p13 chr2: 42,580,484-42,580,484 , GRCh38.p12 chr2: 42,353,344-42,353,344 COX7A2L
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7041290inversion1nstd229human GRCh38 chr2: 41,299,652-42,501,090 , GRCh37.p13 chr2: 41,526,792-42,728,230 RPS13P3, EML4-AS1, 15 more genes
    nsv7039759inversion1nstd229human GRCh38 chr2: 39,986,388-47,339,194 , GRCh37.p13 chr2: 40,213,528-47,566,333 RPL36AP14, CRIPT, 105 more genes
    nsv6676566copy number variation1nstd229human GRCh38 chr2: 42,289,787-42,341,436 , GRCh37.p13 chr2: 42,516,927-42,568,576 COX7A2L, EML4
    nsv6675226copy number variation1nstd229human GRCh38 chr2: 42,345,801-42,376,800 , GRCh37.p13 chr2: 42,572,941-42,603,940 COX7A2L
    nsv6674337copy number variation1nstd229human GRCh38 chr2: 42,335,086-42,366,196 , GRCh37.p13 chr2: 42,562,226-42,593,336 COX7A2L
    nsv6671316copy number variation1nstd229human GRCh38 chr2: 42,355,000-42,355,220 , GRCh37.p13 chr2: 42,582,140-42,582,360 COX7A2L
    nsv6667212copy number variation1nstd229human GRCh38 chr2: 42,347,089-42,350,732 , GRCh37.p13 chr2: 42,574,229-42,577,872 COX7A2L
    nsv6666664copy number variation1nstd229human GRCh38 chr2: 42,346,901-42,379,100 , GRCh37.p13 chr2: 42,574,041-42,606,240 COX7A2L
    nsv6664978copy number variation1nstd229human GRCh38 chr2: 42,320,479-42,336,859 , GRCh37.p13 chr2: 42,547,619-42,563,999 EML4, COX7A2L
    nsv6664462copy number variation1nstd229human GRCh38 chr2: 42,331,701-42,339,400 , GRCh37.p13 chr2: 42,558,841-42,566,540 COX7A2L, EML4
    nsv6663255copy number variation1nstd229human GRCh38 chr2: 42,220,801-42,363,254 , GRCh37.p13 chr2: 42,447,941-42,590,394 EML4, COX7A2L
    nsv6659204copy number variation1nstd229human GRCh38 chr2: 42,332,901-42,389,300 , GRCh37.p13 chr2: 42,560,041-42,616,440 EML4, COX7A2L
    nsv6658961copy number variation1nstd229human GRCh38 chr2: 42,350,488-42,360,283 , GRCh37.p13 chr2: 42,577,628-42,587,423 COX7A2L
    nsv6658391copy number variation1nstd229human GRCh38 chr2: 42,288,901-43,411,600 , GRCh37.p13 chr2: 42,516,041-43,638,739 LOC112268413, RNU6-958P, 22 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6627858copy number variation1nstd224human GRCh37 chr2: 41,848,835-42,594,646 , GRCh38.p12 chr2: 41,621,695-42,367,506 COX7A2L, LINC01913, 10 more genes
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