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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977326inversion1nstd209human GRCh38 chr5: 176,286,704-177,635,736 , GRCh37.p13 chr5: 175,713,707-177,062,737 , CLTB, 46 more genes
    nsv5894695copy number variation1nstd209human GRCh38 chr5: 177,486,764-177,487,059 , GRCh37.p13 chr5: 176,913,765-176,914,060 PDLIM7
    nsv5890062copy number variation1nstd209human GRCh38 chr5: 176,061,658-178,007,127 , GRCh37.p13 chr5: 175,488,661-177,434,128 , DBN1, 65 more genes
    nsv5559468inversion1nstd206human GRCh38 chr5: 177,496,560-177,496,700 , GRCh37.p13 chr5: 176,923,561-176,923,701 PDLIM7
    nsv5458637copy number variation1nstd206human GRCh38 chr5: 177,486,764-177,487,060 , GRCh37.p13 chr5: 176,913,765-176,914,061 PDLIM7
    nsv5369105translocation1nstd200human GRCh38 chr10: 32,511,802-32,511,802 , GRCh38 chr5: 177,487,574-177,487,574 , GRCh37.p13 chr10: 32,800,730-32,800,730 , GRCh37.p13 chr5: 176,914,575-176,914,575 PDLIM7, CCDC7, 1 more genes
    nsv5232677copy number variation1nstd204human GRCh38.p13 chr5: 177,340,901-177,518,700 , GRCh37.p13 chr5: 176,767,902-176,945,701 , FAM193B, 13 more genes
    nsv5197862mobile element insertion1nstd203human GRCh38 chr5: 177,493,601-177,493,616 , GRCh37.p13 chr5: 176,920,602-176,920,617 PDLIM7
    nsv5040815inversion1nstd200human GRCh38 chr5: 177,496,560-177,496,692 , GRCh37.p13 chr5: 176,923,561-176,923,693 PDLIM7
    nsv4882625inversion1nstd200human GRCh37 chr5: 176,923,564-176,923,694 , GRCh38.p12 chr5: 177,496,563-177,496,693 PDLIM7
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4765127inversion1nstd199human GRCh37 chr5: 175,457,760-177,239,501 , GRCh38.p12 chr5: 176,030,757-177,812,500 , CLTB, 60 more genes
    nsv4764354inversion1nstd199human GRCh37 chr5: 175,368,726-177,329,050 , GRCh38.p12 chr5: 175,941,723-177,902,049 , CLTB, 66 more genes
    nsv4763538inversion1nstd199human GRCh37 chr5: 170,260,689-178,183,120 , GRCh38.p12 chr5: 170,833,685-178,756,119 , BNIP1, 194 more genes
    nsv4763338inversion1nstd199human GRCh37 chr5: 175,460,977-177,237,065 , GRCh38.p12 chr5: 176,033,974-177,810,064 , CLTB, 60 more genes
    nsv4755941inversion1nstd199human GRCh37 chr5: 175,346,194-177,347,044 , GRCh38.p12 chr5: 175,919,191-177,920,043 , CLTB, 66 more genes
    nsv4729600copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,570,677-177,114,151 , GRCh38.p12 chr5: 176,143,674-177,687,150 RNF44, NOP16, 48 more genes
    nsv4729439copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,394,616-177,436,413 , GRCh38.p12 chr5: 175,967,613-178,009,412 KIAA1191, DOK3, 65 more genes
    nsv4685982copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,346,695-177,469,711 , GRCh38.p12 chr5: 175,919,692-178,042,710 NOP16, DDX41, 65 more genes
    nsv4592922copy number variation1nstd183human GRCh37 chr5: 176,776,426-176,946,576 , GRCh38.p12 chr5: 177,349,425-177,519,575 , PRR7, 12 more genes
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