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Items: 1 to 20 of 276

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076534inversion1nstd229human GRCh38 chr9: 14,709,244-14,713,276 , GRCh37.p13 chr9: 14,709,242-14,713,274 CER1
    nsv7072115inversion1nstd229human GRCh38 chr9: 12,276,809-15,153,662 , GRCh37.p13 chr9: 12,276,809-15,153,660 PES1P2, RNU6-559P, 30 more genes
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv7062404inversion1nstd229human GRCh38 chr9: 12,646,715-21,082,028 , GRCh37.p13 chr9: 12,646,715-21,082,027 RPS6, RPL7AP47, 95 more genes
    nsv6877622copy number variation1nstd229human GRCh38 chr9: 14,226,508-15,063,519 , GRCh37.p13 chr9: 14,226,507-15,063,517 LDHAP4, CDCA4P1, 11 more genes
    nsv6872841copy number variation1nstd229human GRCh38 chr9: 14,627,573-14,801,777 , GRCh37.p13 chr9: 14,627,571-14,801,775 CER1, FREM1, 2 more genes
    nsv6867713copy number variation1nstd229human GRCh38 chr9: 14,711,167-14,716,492 , GRCh37.p13 chr9: 14,711,165-14,716,490 CER1
    nsv6863470copy number variation1nstd229human GRCh38 chr9: 14,698,054-14,780,263 , GRCh37.p13 chr9: 14,698,052-14,780,261 FREM1, CER1
    nsv6860421copy number variation1nstd229human GRCh38 chr9: 5,097,512-15,003,390 , GRCh37.p13 chr9: 5,097,512-15,003,388 LOC102724027, ATP5PDP3, 89 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
    nsv6634450copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-15,048,247 , GRCh38.p12 chr9: 203,861-15,048,249 LOC102724027, DMRT2, 157 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
    nsv6633232copy number variation1nstd224human GRCh37 chr9: 14,281,387-14,885,180 , GRCh38.p12 chr9: 14,281,388-14,885,182 NFIB, CER1, 6 more genes
    nsv6564848inversion1nstd223human GRCh38 chr9: 12,646,715-21,082,031 , GRCh37.p13 chr9: 12,646,715-21,082,030 LOC105375988, CLK3P1, 95 more genes
    nsv6424375copy number variation1nstd223human GRCh38 chr9: 14,722,700-14,724,935 , GRCh37.p13 chr9: 14,722,698-14,724,933 CER1
    nsv6416465copy number variation1nstd223human GRCh38 chr9: 14,710,901-14,713,800 , GRCh37.p13 chr9: 14,710,899-14,713,798 CER1
    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
    nsv6315395copy number variation1nstd102humanPathogenic GRCh37 chr9: 4,992,582-19,322,101 , GRCh38.p12 chr9: 4,992,582-19,322,103 FREM1, SNAPC3, 142 more genes
    nsv6313892copy number variation1nstd102humanPathogenic GRCh37 chr9: 676,264-33,743,670 , GRCh38.p12 chr9: 676,264-33,743,672 SUGT1P1, FOCAD-AS1, 391 more genes
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