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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098451copy number variation1nstd102humanUncertain significance GRCh37 chr9: 26,946,875-27,109,660 , GRCh38.p12 chr9: 26,946,877-27,109,662 PLAA, IFT74-AS1, 3 more genes
    nsv7098077copy number variation1nstd102humanUncertain significance GRCh37 chr9: 26,934,991-27,220,163 , GRCh38.p12 chr9: 26,934,993-27,220,165 IFT74, LRRC19, 5 more genes
    nsv7098076copy number variation1nstd102humanUncertain significance GRCh37 chr9: 26,905,509-27,018,705 , GRCh38.p12 chr9: 26,905,511-27,018,707 IFT74-AS1, LRRC19, 2 more genes
    nsv7077127inversion1nstd229human GRCh38 chr9: 26,819,519-26,974,122 , GRCh37.p13 chr9: 26,819,517-26,974,120 IFT74-AS1, PLAA, 3 more genes
    nsv7065397inversion1nstd229human GRCh38 chr9: 26,730,468-27,225,878 , GRCh37.p13 chr9: 26,730,466-27,225,876 RPL36AP34, LRRC19, 8 more genes
    nsv7063062inversion1nstd229human GRCh38 chr9: 22,592,329-32,576,343 , GRCh37.p13 chr9: 22,592,328-32,576,341 HSPA8P17, RMRPP5, 81 more genes
    nsv6877354copy number variation1nstd229human GRCh38 chr9: 26,898,708-26,993,115 , GRCh37.p13 chr9: 26,898,706-26,993,113 IFT74-AS1, LRRC19, 2 more genes
    nsv6875942copy number variation1nstd229human GRCh38 chr9: 24,741,564-30,889,392 , GRCh37.p13 chr9: 24,741,562-30,889,390 IFNK, LINC01242, 46 more genes
    nsv6875822copy number variation1nstd229human GRCh38 chr9: 26,950,480-26,956,390 , GRCh37.p13 chr9: 26,950,478-26,956,388 IFT74-AS1, IFT74
    nsv6873758copy number variation1nstd229human GRCh38 chr9: 26,952,226-26,953,929 , GRCh37.p13 chr9: 26,952,224-26,953,927 IFT74, IFT74-AS1
    nsv6863369copy number variation1nstd229human GRCh38 chr9: 26,879,901-27,112,800 , GRCh37.p13 chr9: 26,879,899-27,112,798 PLAA, LRRC19, 5 more genes
    nsv6861503copy number variation1nstd229human GRCh38 chr9: 26,680,968-27,607,029 , GRCh37.p13 chr9: 26,680,966-27,607,027 CTAGE12P, LOC105369289, 16 more genes
    nsv6858442copy number variation1nstd229human GRCh38 chr9: 26,943,606-27,137,458 , GRCh37.p13 chr9: 26,943,604-27,137,456 TEK, IFT74-AS1, 3 more genes
    nsv6858374copy number variation1nstd229human GRCh38 chr9: 26,361,382-26,970,723 , GRCh37.p13 chr9: 26,361,380-26,970,721 IFT74-AS1, LOC105376000, 7 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6562498inversion1nstd223human GRCh38 chr9: 20,655,689-27,693,631 , GRCh37.p13 chr9: 20,655,688-27,693,629 IFNA7, IFNW1, 92 more genes
    nsv6419095copy number variation1nstd223human GRCh38 chr9: 26,431,316-27,005,976 , GRCh37.p13 chr9: 26,431,314-27,005,974 LOC105369289, LRRC19, 8 more genes
    nsv6315463copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-35,903,398 , GRCh38.p12 chr9: 203,861-35,903,401 IFNA11P, RNU6-14P, 495 more genes
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 more genes
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