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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5453236copy number variation1nstd206human GRCh38 chr3: 32,497,150-32,497,626 , GRCh37.p13 chr3: 32,538,642-32,539,118 CMTM6
    nsv5449729copy number variation1nstd206human GRCh38 chr3: 32,495,730-32,500,829 , GRCh37.p13 chr3: 32,537,222-32,542,321 CMTM6
    nsv5447920copy number variation1nstd206human GRCh38 chr3: 32,497,500-32,497,562 , GRCh37.p13 chr3: 32,538,992-32,539,054 CMTM6
    nsv5071169mobile element insertion1nstd203human GRCh38 chr3: 32,497,977-32,497,992 , GRCh37.p13 chr3: 32,539,469-32,539,484 CMTM6
    nsv5062551mobile element insertion1nstd203human GRCh38 chr3: 32,497,984-32,497,992 , GRCh37.p13 chr3: 32,539,476-32,539,484 CMTM6
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4793920copy number variation1nstd200human GRCh37 chr3: 32,391,980-33,567,070 , GRCh38.p12 chr3: 32,350,488-33,525,578 , RPL30P4, 25 more genes
    nsv4734422copy number variation1nstd199human GRCh37 chr3: 32,538,632-32,539,112 , GRCh38.p12 chr3: 32,497,140-32,497,620 CMTM6
    nsv4573205sequence alteration1nstd166human GRCh37.p13 chr3: 32,133,486-32,546,433 , GRCh38.p12 chr3: 32,091,994-32,504,941 GPD1L, CMTM6, 5 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4555873insertion1nstd166human GRCh37.p13 chr3: 32,529,281-32,529,281 , GRCh38.p12 chr3: 32,487,789-32,487,789 CMTM6
    nsv4470534mobile element insertion1nstd166human GRCh37.p13 chr3: 32,539,469-32,539,469 , GRCh38.p12 chr3: 32,497,977-32,497,977 CMTM6
    nsv4085649copy number variation1nstd166human GRCh37.p13 chr3: 32,320,947-32,538,596 , GRCh38.p12 chr3: 32,279,455-32,497,104 CMTM7, CMTM8, 1 more genes
    nsv4083798copy number variation1nstd166human GRCh37.p13 chr3: 32,537,222-32,542,321 , GRCh38.p12 chr3: 32,495,730-32,500,829 CMTM6
    nsv3923656copy number variation1nstd102humanPathogenic GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034 RN7SL4P, TOP2B, 348 more genes
    nsv3918147copy number variation1nstd102humanPathogenic GRCh38 chr3: 32,322,382-36,775,606 , NCBI36 chr3: 32,338,878-36,792,101 , GRCh37 chr3: 32,363,874-36,817,097 TRIM71, CMTM8, 46 more genes
    nsv3913369copy number variation1nstd102humanPathogenic NCBI36 chr3: 29,206,432-35,025,542 , GRCh37.p13 chr3: 29,231,428-35,050,538 , GRCh38.p12 chr3: 29,189,937-35,009,046 MTND4LP9, FNBP1P2, 61 more genes
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