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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097947copy number variation1nstd102humanUncertain significance GRCh37 chr9: 21,974,667-22,160,087 , GRCh38.p12 chr9: 21,974,668-22,160,088 CDKN2B, UBA52P6, 2 more genes
    nsv7070982inversion1nstd229human GRCh38 chr9: 21,712,264-26,561,982 , GRCh37.p13 chr9: 21,712,263-26,561,980 LOC100419692, GARIN3P1, 32 more genes
    nsv6877388copy number variation1nstd229human GRCh38 chr9: 21,310,217-22,111,393 , GRCh37.p13 chr9: 21,310,216-22,111,392 UBA52P6, KHSRPP1, 23 more genes
    nsv6874507copy number variation1nstd229human GRCh38 chr9: 21,937,413-22,077,540 , GRCh37.p13 chr9: 21,937,412-22,077,539 CDKN2B, CDKN2A-AS1, 3 more genes
    nsv6869765copy number variation1nstd229human GRCh38 chr9: 21,997,897-22,001,255 , GRCh37.p13 chr9: 21,997,896-22,001,254 CDKN2B-AS1, CDKN2B
    nsv6861775copy number variation1nstd229human GRCh38 chr9: 21,652,201-23,305,600 , GRCh37.p13 chr9: 21,652,200-23,305,598 LOC107987026, DMRTA1, 12 more genes
    nsv6637750copy number variation1nstd102humanUncertain significance GRCh37 chr9: 20,659,492-22,347,440 , GRCh38.p12 chr9: 20,659,493-22,347,441 CDKN2B, IFNA10, 46 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
    nsv6418132copy number variation1nstd223human GRCh38 chr9: 21,937,413-22,077,537 , GRCh37.p13 chr9: 21,937,412-22,077,536 CDKN2A-AS1, CDKN2A, 3 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
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 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
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 more genes
    nsv6313697copy number variation1nstd102humanPathogenic GRCh37 chr9: 21,902,071-22,015,434 , GRCh38.p12 chr9: 21,902,072-22,015,435 CDKN2B, CDKN2A, 3 more genes
    nsv6313553copy number variation1nstd102humanUncertain significance GRCh37 chr9: 22,003,967-30,712,948 , GRCh38.p12 chr9: 22,003,968-30,712,950 ME2P1, NOP56P2, 61 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6313095copy number variation1nstd102humanUncertain significance GRCh37 chr9: 21,994,128-22,160,087 , GRCh38.p12 chr9: 21,994,129-22,160,088 CDKN2B-AS1, CDKN2B, 2 more genes
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