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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6876635copy number variation1nstd229human GRCh38 chr9: 72,384,161-74,793,192 , GRCh37.p13 chr9: 74,999,077-77,408,108 LOC101927329, LOC100289351, 27 more genes
    nsv6859693copy number variation1nstd229human GRCh38 chr9: 74,269,541-74,698,518 , GRCh37.p13 chr9: 76,884,457-77,313,434 RORB, RORB-AS1, 4 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
    nsv6443035copy number variation1nstd223human GRCh38 chr9: 74,374,363-74,374,696 , GRCh37.p13 chr9: 76,989,279-76,989,612 LOC101927358
    nsv6436286copy number variation1nstd223human GRCh38 chr9: 74,383,958-74,384,513 , GRCh37.p13 chr9: 76,998,874-76,999,429 LOC101927358
    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
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 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
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6257752mobile element insertion1nstd215human GRCh38 chr9: 74,372,120-74,372,120 , GRCh37.p13 chr9: 76,987,036-76,987,036 LOC101927358
    nsv6147016sequence alteration1nstd206human GRCh38 chr9: 74,371,472-74,378,348 , GRCh37.p13 chr9: 76,986,388-76,993,264 LOC101927358, LOC105376087
    nsv6137094copy number variation1nstd213human GRCh37 chr9: 71,840,000-78,800,001 , GRCh38.p12 chr9: 69,225,084-76,185,085 KLF9, PCSK5, 83 more genes
    nsv4546727insertion1nstd166human GRCh37.p13 chr9: 76,990,687-76,990,687 , GRCh38.p12 chr9: 74,375,771-74,375,771 LOC101927358
    nsv4485051mobile element insertion1nstd166human GRCh37.p13 chr9: 76,996,722-76,996,722 , GRCh38.p12 chr9: 74,381,806-74,381,806 LOC101927358
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456476copy number variation1nstd102humanUncertain significance GRCh37 chr9: 76,268,525-77,162,885 , GRCh38.p12 chr9: 73,653,609-74,547,969 RNA5SP286, RORB-AS1, 6 more genes
    nsv4455928copy number variation1nstd102humanPathogenic GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877 RPL35AP21, LOC105376097, 134 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 more genes
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