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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068863inversion1nstd229human GRCh38 chr13: 27,564,614-31,455,391 , GRCh37.p13 chr13: 28,138,751-32,029,528 MFAP1P1, RN7SL272P, 70 more genes
    nsv6935031copy number variation1nstd229human GRCh38 chr13: 27,934,133-27,954,572 , GRCh37.p13 chr13: 28,508,270-28,528,709 LINC00543, ATP5F1EP2
    nsv6932013copy number variation1nstd229human GRCh38 chr13: 27,894,801-28,169,500 , GRCh37.p13 chr13: 28,468,938-28,743,637 URAD, CDX2, 12 more genes
    nsv6925525copy number variation1nstd229human GRCh38 chr13: 27,942,731-27,957,834 , GRCh37.p13 chr13: 28,516,868-28,531,971 LINC00543, ATP5F1EP2
    nsv6921502copy number variation1nstd229human GRCh38 chr13: 27,942,367-27,946,911 , GRCh37.p13 chr13: 28,516,504-28,521,048 ATP5F1EP2
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6492920copy number variation1nstd223human GRCh38 chr13: 27,942,731-27,957,830 , GRCh37.p13 chr13: 28,516,868-28,531,967 LINC00543, ATP5F1EP2
    nsv6492129copy number variation1nstd223human GRCh38 chr13: 27,934,133-27,954,572 , GRCh37.p13 chr13: 28,508,270-28,528,709 LINC00543, ATP5F1EP2
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6132752copy number variation1nstd213human GRCh37 chr13: 27,480,000-28,970,001 , GRCh38.p12 chr13: 26,905,863-28,395,864 CDX2, FLT1, 41 more genes
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6132475copy number variation1nstd213human GRCh37 chr13: 26,620,000-32,650,001 , GRCh38.p12 chr13: 26,045,862-32,075,864 ALOX5AP, HMGB1, 106 more genes
    nsv5942494copy number variation1nstd209human GRCh38 chr13: 27,934,133-27,954,571 , GRCh37.p13 chr13: 28,508,270-28,528,708 ATP5F1EP2, LINC00543
    nsv5850864copy number variation1nstd209human GRCh38 chr13: 27,934,203-27,954,352 , GRCh37.p13 chr13: 28,508,340-28,528,489 LINC00543, ATP5F1EP2
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5512786copy number variation1nstd206human GRCh38 chr13: 27,934,133-27,954,572 , GRCh37.p13 chr13: 28,508,270-28,528,709 LINC00543, ATP5F1EP2
    nsv5314216copy number variation1nstd204human GRCh38.p13 chr13: 27,934,132-27,954,573 , GRCh37.p13 chr13: 28,508,269-28,528,710 LINC00543, ATP5F1EP2
    nsv5280343copy number variation1nstd204human GRCh38.p13 chr13: 27,932,360-27,954,189 , GRCh37.p13 chr13: 28,506,497-28,528,326 LINC00543, ATP5F1EP2
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