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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946313copy number variation1nstd209human GRCh38 chr17: 42,578,501-42,578,574 , GRCh37.p13 chr17: 40,730,519-40,730,592 RETREG3
    nsv5883061copy number variation1nstd209human GRCh38 chr17: 42,589,488-42,591,237 , GRCh37.p13 chr17: 40,741,506-40,743,255 RETREG3
    nsv5703655mobile element insertion1nstd211human GRCh38 chr17: 42,597,608-42,597,608 , GRCh37.p13 chr17: 40,749,626-40,749,626 RETREG3
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5524321copy number variation1nstd206human GRCh38 chr17: 42,596,305-42,601,558 , GRCh37.p13 chr17: 40,748,323-40,753,576 RETREG3
    nsv5298058copy number variation1nstd204human GRCh38.p13 chr17: 42,595,362-42,597,684 , GRCh37.p13 chr17: 40,747,380-40,749,702 RETREG3
    nsv5293339copy number variation1nstd204human GRCh38.p13 chr17: 42,464,901-42,659,200 , GRCh37.p13 chr17: 40,616,919-40,811,218 ATP5MGP7, PTP4A2P1, 14 more genes
    nsv5280442copy number variation1nstd204human GRCh38.p13 chr17: 42,596,862-42,601,089 , GRCh37.p13 chr17: 40,748,880-40,753,107 RETREG3
    nsv5209042mobile element deletion1nstd204human GRCh38.p13 chr17: 42,606,361-42,606,631 , GRCh37.p13 chr17: 40,758,379-40,758,649 RETREG3
    nsv5157840mobile element insertion1nstd203human GRCh38 chr17: 42,602,521-42,602,534 , GRCh37.p13 chr17: 40,754,539-40,754,552 RETREG3
    nsv5016437copy number variation1nstd200human GRCh38 chr17: 42,596,335-42,601,529 , GRCh37.p13 chr17: 40,748,353-40,753,547 RETREG3
    nsv5016436copy number variation1nstd200human GRCh38 chr17: 42,573,892-42,577,673 , GRCh37.p13 chr17: 40,725,910-40,729,691 PSMC3IP, RETREG3
    nsv5013718copy number variation1nstd200human GRCh38 chr17: 42,593,536-42,601,597 , GRCh37.p13 chr17: 40,745,554-40,753,615 RETREG3
    nsv4867032copy number variation1nstd200human GRCh37 chr17: 40,748,353-40,753,547 , GRCh38.p12 chr17: 42,596,335-42,601,529 RETREG3
    nsv4867031copy number variation1nstd200human GRCh37 chr17: 40,746,844-40,747,015 , GRCh38.p12 chr17: 42,594,826-42,594,997 RETREG3
    nsv4867030copy number variation1nstd200human GRCh37 chr17: 40,745,514-40,753,325 , GRCh38.p12 chr17: 42,593,496-42,601,307 RETREG3
    nsv4786199mobile element deletion1nstd200human GRCh37 chr17: 40,758,388-40,758,643 , GRCh38.p12 chr17: 42,606,370-42,606,625 RETREG3
    nsv4733124copy number variation1nstd199human GRCh37 chr17: 40,730,517-40,730,588 , GRCh38.p12 chr17: 42,578,499-42,578,570 RETREG3
    nsv4631683copy number variation1nstd183human GRCh37 chr17: 40,579,816-40,758,733 , GRCh38.p12 chr17: 42,427,798-42,606,715 RETREG3, MIR548AT, 12 more genes
    nsv4457627copy number variation1nstd102humanUncertain significance GRCh37 chr17: 40,595,473-40,785,031 , GRCh38.p12 chr17: 42,443,455-42,633,013 HSD17B1, RETREG3, 11 more genes
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