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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7069439inversion1nstd229human GRCh38 chr10: 10,500,497-12,439,947 , GRCh37.p13 chr10: 10,542,460-12,481,946 LOC105376409, SFTA1P, 26 more genes
    nsv7061969inversion1nstd229human GRCh38 chr10: 11,128,019-14,526,691 , GRCh37.p13 chr10: 11,169,982-14,568,690 RPL5P25, LOC105376425, 58 more genes
    nsv6894506copy number variation1nstd229human GRCh38 chr10: 11,759,026-11,783,568 , GRCh37.p13 chr10: 11,801,025-11,825,567 LOC105376415, LOC105379850, 1 more genes
    nsv6892087copy number variation1nstd229human GRCh38 chr10: 11,760,235-11,768,088 , GRCh37.p13 chr10: 11,802,234-11,810,087 ECHDC3
    nsv6886071copy number variation1nstd229human GRCh38 chr10: 11,753,867-11,760,863 , GRCh37.p13 chr10: 11,795,866-11,802,862 ECHDC3
    nsv6880886copy number variation1nstd229human GRCh38 chr10: 11,746,056-11,748,847 , GRCh37.p13 chr10: 11,788,055-11,790,846 ECHDC3
    nsv6878498copy number variation1nstd229human GRCh38 chr10: 11,762,551-11,765,206 , GRCh37.p13 chr10: 11,804,550-11,807,205 ECHDC3
    nsv6637939copy number variation1nstd102humanUncertain significance GRCh37 chr10: 100,027-12,648,149 , GRCh38.p12 chr10: 54,087-12,606,150 LARP4B-DT, CALML5, 206 more genes
    nsv6637717copy number variation1nstd102humanUncertain significance GRCh37 chr10: 11,713,298-11,897,052 , GRCh38.p12 chr10: 11,671,299-11,855,053 ECHDC3, PROSER2-AS1, 5 more genes
    nsv6447693copy number variation1nstd223human GRCh38 chr10: 11,753,867-11,760,860 , GRCh37.p13 chr10: 11,795,866-11,802,859 ECHDC3
    nsv6436832copy number variation1nstd223human GRCh38 chr10: 11,759,026-11,783,567 , GRCh37.p13 chr10: 11,801,025-11,825,566 LOC105379850, LOC105376415, 1 more genes
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6131971copy number variation1nstd213human GRCh37 chr10: 7,450,000-17,830,001 , GRCh38.p12 chr10: 7,408,038-17,788,002 ATP5F1C, TRDMT1, 150 more genes
    nsv6094008insertion1nstd212human GRCh38 chr10: 11,742,342-11,742,342 , GRCh37.p13 chr10: 11,784,341-11,784,341 ECHDC3
    nsv5730874mobile element insertion2nstd211human GRCh38 chr10: 11,750,741-11,750,741 , GRCh37.p13 chr10: 11,792,740-11,792,740 ECHDC3
    nsv5630581insertion1nstd207human GRCh38 chr10: 11,742,311-11,742,311 , GRCh37.p13 chr10: 11,784,310-11,784,310 ECHDC3
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5186866mobile element insertion1nstd203human GRCh38 chr10: 11,750,730-11,750,741 , GRCh37.p13 chr10: 11,792,729-11,792,740 ECHDC3
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