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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095431copy number variation1nstd102humanUncertain significance GRCh37 chr18: 18,963,480-21,534,612 , GRCh38.p12 chr18: 21,383,519-23,954,648 MIB1, RN7SL233P, 41 more genes
    nsv7095003copy number variation1nstd102humanPathogenic GRCh37 chr18: 21,508,077-21,508,739 , GRCh38.p12 chr18: 23,928,113-23,928,775 LAMA3
    nsv7095002copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 21,473,162-21,481,161 , GRCh38.p12 chr18: 23,893,198-23,901,197 LAMA3
    nsv7071653inversion1nstd229human GRCh38 chr18: 23,834,902-23,837,150 , GRCh37.p13 chr18: 21,414,866-21,417,114 LAMA3
    nsv7068113inversion1nstd229human GRCh38 chr18: 23,802,062-23,802,111 , GRCh37.p13 chr18: 21,382,026-21,382,075 LAMA3
    nsv7064470inversion1nstd229human GRCh38 chr18: 23,699,337-23,699,356 , GRCh37.p13 chr18: 21,279,301-21,279,320 LAMA3
    nsv7058839inversion1nstd229human GRCh38 chr18: 23,828,438-23,869,346 , GRCh37.p13 chr18: 21,408,402-21,449,310 LAMA3
    nsv7017772copy number variation1nstd229human GRCh38 chr18: 23,899,932-23,900,453 , GRCh37.p13 chr18: 21,479,896-21,480,417 LAMA3
    nsv7015698copy number variation1nstd229human GRCh38 chr18: 23,878,410-23,880,391 , GRCh37.p13 chr18: 21,458,374-21,460,355 LAMA3
    nsv7014588copy number variation1nstd229human GRCh38 chr18: 23,884,077-23,884,100 , GRCh37.p13 chr18: 21,464,041-21,464,064 LAMA3
    nsv7014057copy number variation1nstd229human GRCh38 chr18: 23,950,330-23,950,405 , GRCh37.p13 chr18: 21,530,294-21,530,369 LAMA3
    nsv7013160copy number variation1nstd229human GRCh38 chr18: 23,715,228-23,720,971 , GRCh37.p13 chr18: 21,295,192-21,300,935 LAMA3
    nsv7012770copy number variation1nstd229human GRCh38 chr18: 23,925,876-23,930,079 , GRCh37.p13 chr18: 21,505,840-21,510,043 LAMA3
    nsv7011947copy number variation1nstd229human GRCh38 chr18: 23,735,230-23,740,169 , GRCh37.p13 chr18: 21,315,194-21,320,133 LAMA3
    nsv7009795copy number variation1nstd229human GRCh38 chr18: 23,936,120-23,940,204 , GRCh37.p13 chr18: 21,516,084-21,520,168 LAMA3
    nsv7007856copy number variation1nstd229human GRCh38 chr18: 23,760,818-23,765,838 , GRCh37.p13 chr18: 21,340,782-21,345,802 LAMA3
    nsv7006880copy number variation1nstd229human GRCh38 chr18: 23,757,525-23,780,376 , GRCh37.p13 chr18: 21,337,489-21,360,340 LAMA3
    nsv7006867copy number variation1nstd229human GRCh38 chr18: 23,679,029-23,764,092 , GRCh37.p13 chr18: 21,258,993-21,344,056 RPL23AP77, LAMA3
    nsv7006336copy number variation1nstd229human GRCh38 chr18: 23,857,956-23,866,264 , GRCh37.p13 chr18: 21,437,920-21,446,228 LAMA3
    nsv7006125copy number variation1nstd229human GRCh38 chr18: 23,701,128-23,714,022 , GRCh37.p13 chr18: 21,281,092-21,293,986 LAMA3, RPL23AP77
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