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Items: 1 to 20 of 88

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048266inversion1nstd229human GRCh38 chr3: 26,811,879-28,628,249 , GRCh37.p13 chr3: 26,853,370-28,669,740 RNU1-96P, KIAA1143P2, 22 more genes
    nsv7041296inversion1nstd229human GRCh38 chr3: 26,495,717-29,400,966 , GRCh37.p13 chr3: 26,537,208-29,442,457 CIAO2AP1, RNU6-342P, 29 more genes
    nsv6715446copy number variation1nstd229human GRCh38 chr3: 27,818,701-27,829,100 , GRCh37.p13 chr3: 27,860,192-27,870,591 LINC01980, LINC01981
    nsv6711339copy number variation1nstd229human GRCh38 chr3: 26,974,287-30,027,565 , GRCh37.p13 chr3: 27,015,778-30,069,056 LINC01967, TPM4P2, 29 more genes
    nsv6628583copy number variation1nstd224human GRCh37 chr3: 27,743,934-28,531,268 , GRCh38.p12 chr3: 27,702,443-28,489,777 LINC01981, LINC02084, 10 more genes
    nsv6368641copy number variation1nstd223human GRCh38 chr3: 27,832,343-27,832,845 , GRCh37.p13 chr3: 27,873,834-27,874,336 LINC01980, LINC01981
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv5899785copy number variation1nstd209human GRCh38 chr3: 26,482,972-28,493,095 , GRCh37.p13 chr3: 26,524,463-28,534,586 , MICOS10P3, 24 more genes
    nsv5679928mobile element insertion1nstd211human GRCh38 chr3: 27,832,681-27,832,681 , GRCh37.p13 chr3: 27,874,172-27,874,172 LINC01980, LINC01981
    nsv5612653insertion1nstd207human GRCh38 chr3: 27,832,671-27,832,671 , GRCh37.p13 chr3: 27,874,162-27,874,162 LINC01980, LINC01981
    nsv5401553mobile element insertion1nstd206human GRCh38 chr3: 27,832,681-27,832,732 , GRCh37.p13 chr3: 27,874,172-27,874,223 LINC01980, LINC01981
    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
    nsv4924274copy number variation1nstd200human GRCh38 chr3: 27,018,297-28,220,452 , GRCh37.p13 chr3: 27,059,788-28,261,943 , SLC4A7, 17 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
    nsv4674536copy number variation1nstd102humanUncertain significance GRCh37 chr3: 25,901,794-29,520,717 , GRCh38.p12 chr3: 25,860,303-29,479,226 KIAA1143P2, LINC01981, 35 more genes
    nsv4588515copy number variation1nstd183human GRCh37 chr3: 27,873,979-27,882,560 , GRCh38.p12 chr3: 27,832,488-27,841,069 LINC01981, LINC01980
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4542159insertion1nstd166human GRCh37.p13 chr3: 27,874,162-27,874,162 , GRCh38.p12 chr3: 27,832,671-27,832,671 LINC01981, LINC01980
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