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Items: 1 to 20 of 276

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097848copy number variation1nstd102humanUncertain significance GRCh37 chr6: 75,833,644-75,847,315 , GRCh38.p12 chr6: 75,123,928-75,137,599 COL12A1, SNORD156
    nsv7097590copy number variation1nstd102humanUncertain significance GRCh37 chr6: 75,858,054-75,912,508 , GRCh38.p12 chr6: 75,148,338-75,202,792 COL12A1
    nsv7093461delins1nstd102humanUncertain significance GRCh38 chr6: 75,181,157-75,181,158 , GRCh37 chr6: 75,890,873-75,890,874 COL12A1
    nsv7093454delins1nstd102humanLikely pathogenic GRCh38 chr6: 75,102,633-75,102,707 , GRCh37 chr6: 75,812,349-75,812,423 COL12A1
    nsv7048284inversion1nstd229human GRCh38 chr6: 73,272,579-75,940,581 , GRCh37.p13 chr6: 73,982,302-76,650,298 RPL39P3, KHDC1, 45 more genes
    nsv7046565inversion1nstd229human GRCh38 chr6: 75,199,073-75,208,643 , GRCh37.p13 chr6: 75,908,789-75,918,359 COL12A1
    nsv6796014copy number variation1nstd229human GRCh38 chr6: 75,182,482-75,224,470 , GRCh37.p13 chr6: 75,892,198-75,934,186 COL12A1
    nsv6795214copy number variation1nstd229human GRCh38 chr6: 75,159,601-75,163,800 , GRCh37.p13 chr6: 75,869,317-75,873,516 COL12A1
    nsv6794182copy number variation1nstd229human GRCh38 chr6: 75,202,835-75,203,017 , GRCh37.p13 chr6: 75,912,551-75,912,733 COL12A1
    nsv6793507copy number variation1nstd229human GRCh38 chr6: 75,071,024-75,128,959 , GRCh37.p13 chr6: 75,780,740-75,838,675 SNORD156, COL12A1
    nsv6793334copy number variation1nstd229human GRCh38 chr6: 75,167,901-75,266,600 , GRCh37.p13 chr6: 75,877,617-75,976,316 TMEM30A, COL12A1, 1 more genes
    nsv6792996copy number variation1nstd229human GRCh38 chr6: 75,167,879-75,168,070 , GRCh37.p13 chr6: 75,877,595-75,877,786 COL12A1
    nsv6792566copy number variation1nstd229human GRCh38 chr6: 74,836,535-77,129,191 , GRCh37.p13 chr6: 75,546,251-77,838,908 NUP50P4, COX7A2, 29 more genes
    nsv6791746copy number variation1nstd229human GRCh38 chr6: 75,119,088-75,119,523 , GRCh37.p13 chr6: 75,828,804-75,829,239 COL12A1
    nsv6791441copy number variation1nstd229human GRCh38 chr6: 75,206,293-75,213,656 , GRCh37.p13 chr6: 75,916,009-75,923,372 COL12A1
    nsv6791326copy number variation1nstd229human GRCh38 chr6: 74,695,596-75,216,386 , GRCh37.p13 chr6: 75,405,312-75,926,102 NUP50P4, COL12A1, 2 more genes
    nsv6783775copy number variation1nstd229human GRCh38 chr6: 75,190,948-75,207,837 , GRCh37.p13 chr6: 75,900,664-75,917,553 COL12A1
    nsv6781658copy number variation1nstd229human GRCh38 chr6: 75,108,337-75,120,997 , GRCh37.p13 chr6: 75,818,053-75,830,713 COL12A1
    nsv6778580copy number variation1nstd229human GRCh38 chr6: 75,039,536-75,104,000 , GRCh37.p13 chr6: 75,749,252-75,813,716 COL12A1
    nsv6778397copy number variation1nstd229human GRCh38 chr6: 75,138,250-75,138,630 , GRCh37.p13 chr6: 75,847,966-75,848,346 COL12A1
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