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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147551copy number variation1nstd232human GRCh37.p13 chr6: 54,740,509-54,740,566 , GRCh38.p12 chr6: 54,875,711-54,875,768 FAM83B
    nsv7056373inversion1nstd229human GRCh38 chr6: 54,905,761-54,913,862 , GRCh37.p13 chr6: 54,770,559-54,778,660 FAM83B
    nsv7049684inversion1nstd229human GRCh38 chr6: 54,528,495-55,094,616 , GRCh37.p13 chr6: 54,393,293-54,959,414 RPL10P10, LOC107986606, 4 more genes
    nsv7046216inversion1nstd229human GRCh38 chr6: 54,684,072-54,900,338 , GRCh37.p13 chr6: 54,548,870-54,765,136 FAM83B, LOC107986606, 2 more genes
    nsv7041810inversion1nstd229human GRCh38 chr6: 54,908,314-54,913,559 , GRCh37.p13 chr6: 54,773,112-54,778,357 FAM83B
    nsv6794937copy number variation1nstd229human GRCh38 chr6: 54,884,761-54,885,110 , GRCh37.p13 chr6: 54,749,559-54,749,908 FAM83B
    nsv6793358copy number variation1nstd229human GRCh38 chr6: 54,830,168-54,894,228 , GRCh37.p13 chr6: 54,694,966-54,759,026 FAM83B
    nsv6792124copy number variation1nstd229human GRCh38 chr6: 54,850,101-54,860,100 , GRCh37.p13 chr6: 54,714,899-54,724,898 FAM83B
    nsv6792063copy number variation1nstd229human GRCh38 chr6: 53,604,262-54,850,282 , GRCh37.p13 chr6: 53,469,060-54,715,080 CLNS1AP1, LRRC1, 17 more genes
    nsv6791489copy number variation1nstd229human GRCh38 chr6: 54,895,812-54,905,579 , GRCh37.p13 chr6: 54,760,610-54,770,377 FAM83B
    nsv6791288copy number variation1nstd229human GRCh38 chr6: 54,882,701-54,885,100 , GRCh37.p13 chr6: 54,747,499-54,749,898 FAM83B
    nsv6791025copy number variation1nstd229human GRCh38 chr6: 54,878,901-54,893,100 , GRCh37.p13 chr6: 54,743,699-54,757,898 FAM83B
    nsv6790933copy number variation1nstd229human GRCh38 chr6: 54,897,901-55,582,500 , GRCh37.p13 chr6: 54,762,699-55,447,298 HCRTR2, HMGCLL1, 2 more genes
    nsv6789971copy number variation1nstd229human GRCh38 chr6: 54,811,090-54,878,315 , GRCh37.p13 chr6: 54,675,888-54,743,113 FAM83B
    nsv6789142copy number variation1nstd229human GRCh38 chr6: 54,936,595-54,936,717 , GRCh37.p13 chr6: 54,801,393-54,801,515 FAM83B
    nsv6789106copy number variation1nstd229human GRCh38 chr6: 54,897,722-54,916,324 , GRCh37.p13 chr6: 54,762,520-54,781,122 FAM83B
    nsv6787527copy number variation1nstd229human GRCh38 chr6: 54,801,970-54,861,457 , GRCh37.p13 chr6: 54,666,768-54,726,255 FAM83B, LOC107986606
    nsv6787387copy number variation1nstd229human GRCh38 chr6: 54,850,061-54,855,836 , GRCh37.p13 chr6: 54,714,859-54,720,634 FAM83B
    nsv6787184copy number variation1nstd229human GRCh38 chr6: 54,847,216-54,847,246 , GRCh37.p13 chr6: 54,712,014-54,712,044 FAM83B
    nsv6783339copy number variation1nstd229human GRCh38 chr6: 54,905,076-54,905,120 , GRCh37.p13 chr6: 54,769,874-54,769,918 FAM83B
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