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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145801copy number variation1nstd232human GRCh37.p13 chr19: 50,909,577-50,909,660 , GRCh38.p12 chr19: 50,406,320-50,406,403 POLD1
    nsv7095723copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,905,025-50,906,864 , GRCh38.p12 chr19: 50,401,768-50,403,607 POLD1
    nsv7095722copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,887,648-50,917,146 , GRCh38.p12 chr19: 50,384,391-50,413,889 POLD1
    nsv7095663copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,912,388-50,915,072 , GRCh38.p12 chr19: 50,409,131-50,411,815 POLD1
    nsv7095287copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,887,648-50,902,751 , GRCh38.p12 chr19: 50,384,391-50,399,494 POLD1
    nsv7095219copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,905,040-50,909,085 , GRCh38.p12 chr19: 50,401,783-50,405,828 POLD1
    nsv7093082copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,919,067-50,919,126 , GRCh38 chr19: 50,415,810-50,415,869 POLD1
    nsv7077997inversion1nstd229human GRCh38 chr19: 50,085,764-53,270,581 , GRCh37.p13 chr19: 50,589,021-53,773,834 SNORD88B, ZNF320, 181 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 more genes
    nsv7070284inversion1nstd229human GRCh38 chr19: 50,392,546-50,395,590 , GRCh37.p13 chr19: 50,895,803-50,898,847 POLD1
    nsv7064925inversion1nstd229human GRCh38 chr19: 49,540,460-54,108,860 , GRCh37.p13 chr19: 50,043,717-54,528,887 DPRX, EMC10, 323 more genes
    nsv7015908copy number variation1nstd229human GRCh38 chr19: 50,399,823-50,407,332 , GRCh37.p13 chr19: 50,903,080-50,910,589 POLD1
    nsv7015284copy number variation1nstd229human GRCh38 chr19: 50,386,930-50,387,064 , GRCh37.p13 chr19: 50,890,187-50,890,321 POLD1
    nsv7014701copy number variation1nstd229human GRCh38 chr19: 50,384,235-50,384,262 , GRCh37.p13 chr19: 50,887,492-50,887,519 POLD1
    nsv7005102copy number variation1nstd229human GRCh38 chr19: 50,392,088-50,398,186 , GRCh37.p13 chr19: 50,895,345-50,901,443 POLD1
    nsv7005003copy number variation1nstd229human GRCh38 chr19: 50,409,549-50,415,472 , GRCh37.p13 chr19: 50,912,806-50,918,729 POLD1
    nsv7002617copy number variation1nstd229human GRCh38 chr19: 50,408,265-50,424,239 , GRCh37.p13 chr19: 50,911,522-50,927,496 POLD1, SPIB
    nsv7001770copy number variation1nstd229human GRCh38 chr19: 50,388,737-50,397,801 , GRCh37.p13 chr19: 50,891,994-50,901,058 POLD1
    nsv6637438copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,883,114-51,304,591 , GRCh38.p12 chr19: 50,379,857-50,801,334 SMIM47, LRRC4B, 21 more genes
    nsv6596024inversion1nstd223human GRCh38 chr19: 50,090,965-50,608,546 , GRCh37.p13 chr19: 50,594,222-51,111,803 SNAR-B2, MYH14, 27 more genes
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