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Items: 1 to 20 of 507

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960460insertion1nstd209human GRCh38 chr2: 215,134,553-215,134,553 , GRCh37.p13 chr2: 215,999,276-215,999,276 ABCA12
    nsv5959590insertion1nstd209human GRCh38 chr2: 214,989,178-214,989,178 , GRCh37.p13 chr2: 215,853,902-215,853,902 ABCA12
    nsv5953710insertion1nstd209human GRCh38 chr2: 215,134,251-215,134,251 , GRCh37.p13 chr2: 215,998,974-215,998,974 ABCA12
    nsv5952586insertion1nstd209human GRCh38 chr2: 215,016,582-215,016,582 , GRCh37.p13 chr2: 215,881,306-215,881,306 ABCA12
    nsv5894438copy number variation1nstd209human GRCh38 chr2: 215,107,074-215,107,159 , GRCh37.p13 chr2: 215,971,797-215,971,882 ABCA12
    nsv5726315mobile element insertion1nstd211human GRCh38 chr2: 215,071,234-215,071,234 , GRCh37.p13 chr2: 215,935,957-215,935,957 ABCA12
    nsv5722643mobile element insertion1nstd211human GRCh38 chr2: 214,956,825-214,956,825 , GRCh37.p13 chr2: 215,821,549-215,821,549 SNHG31, ABCA12
    nsv5688354mobile element insertion1nstd211human GRCh38 chr2: 215,119,752-215,119,752 , GRCh37.p13 chr2: 215,984,475-215,984,475 ABCA12
    nsv5622130insertion1nstd207human GRCh38 chr2: 215,134,547-215,134,547 , GRCh37.p13 chr2: 215,999,270-215,999,270 ABCA12
    nsv5610547insertion1nstd207human GRCh38 chr2: 215,134,251-215,134,251 , GRCh37.p13 chr2: 215,998,974-215,998,974 ABCA12
    nsv5605894insertion1nstd207human GRCh38 chr2: 215,134,526-215,134,526 , GRCh37.p13 chr2: 215,999,249-215,999,249 ABCA12
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5558066mobile element insertion1nstd206human GRCh38 chr2: 214,956,825-214,956,876 , GRCh37.p13 chr2: 215,821,549-215,821,600 ABCA12, SNHG31
    nsv5546579insertion1nstd206human GRCh38 chr2: 215,033,256-215,033,278 , GRCh37.p13 chr2: 215,897,980-215,898,002 ABCA12
    nsv5450419copy number variation1nstd206human GRCh38 chr2: 215,053,083-215,053,655 , GRCh37.p13 chr2: 215,917,807-215,918,379 ABCA12
    nsv5441067copy number variation1nstd206human GRCh38 chr2: 215,107,076-215,107,160 , GRCh37.p13 chr2: 215,971,799-215,971,883 ABCA12
    nsv5437084copy number variation1nstd206human GRCh38 chr2: 215,037,824-215,039,758 , GRCh37.p13 chr2: 215,902,548-215,904,482 ABCA12
    nsv5366822translocation1nstd200human GRCh38 chr2: 215,134,605-215,134,605 , GRCh38 chr2: 215,134,317-215,134,317 , GRCh37.p13 chr2: 215,999,328-215,999,328 , GRCh37.p13 chr2: 215,999,040-215,999,040 ABCA12
    nsv5361295translocation1nstd200human GRCh38 chr2: 215,107,076-215,107,076 , GRCh38 chr2: 215,107,160-215,107,160 , GRCh37.p13 chr2: 215,971,799-215,971,799 , GRCh37.p13 chr2: 215,971,883-215,971,883 ABCA12
    nsv5309259copy number variation1nstd204human GRCh38.p13 chr2: 213,306,045-215,346,832 , GRCh37.p13 chr2: 214,170,769-216,211,555 ABCA12, VWC2L, 11 more genes
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