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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076798inversion1nstd229human GRCh38 chr9: 70,397,350-70,398,860 , GRCh37.p13 chr9: 73,012,266-73,013,776 KLF9
    nsv7058411inversion1nstd229human GRCh38 chr9: 70,389,783-70,389,828 , GRCh37.p13 chr9: 73,004,699-73,004,744 KLF9
    nsv6876574copy number variation1nstd229human GRCh38 chr9: 70,407,682-70,410,912 , GRCh37.p13 chr9: 73,022,598-73,025,828 KLF9
    nsv6873470copy number variation1nstd229human GRCh38 chr9: 70,225,601-70,561,100 , GRCh37.p13 chr9: 72,840,517-73,176,016 MAMDC2, KLF9, 5 more genes
    nsv6869816copy number variation1nstd229human GRCh38 chr9: 70,371,751-70,389,734 , GRCh37.p13 chr9: 72,986,667-73,004,650 KLF9
    nsv6862944copy number variation1nstd229human GRCh38 chr9: 70,128,037-70,524,907 , GRCh37.p13 chr9: 72,742,953-73,139,823 LOC105376079, RPL24P8, 7 more genes
    nsv6860782copy number variation1nstd229human GRCh38 chr9: 70,318,749-70,739,208 , GRCh37.p13 chr9: 72,933,665-73,354,124 KLF9, KLF9-DT, 6 more genes
    nsv6637502copy number variation1nstd102humanUncertain significance GRCh37 chr9: 70,966,262-76,901,382 , GRCh38.p12 chr9: 68,351,346-74,286,466 RPS20P24, MAMDC2-AS1, 77 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
    nsv6568574inversion1nstd223human GRCh38 chr9: 70,397,486-70,398,495 , GRCh37.p13 chr9: 73,012,402-73,013,411 KLF9
    nsv6436381copy number variation1nstd223human GRCh38 chr9: 70,412,401-70,414,300 , GRCh37.p13 chr9: 73,027,317-73,029,216 KLF9-DT, KLF9
    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
    nsv6277893insertion1nstd214human GRCh38 chr9: 70,383,197-70,383,197 , GRCh37.p13 chr9: 72,998,113-72,998,113 KLF9
    nsv6266352copy number variation1nstd214human GRCh38 chr9: 70,409,072-70,409,197 , GRCh37.p13 chr9: 73,023,988-73,024,113 KLF9
    nsv6217417insertion1nstd214human GRCh38 chr9: 70,409,141-70,409,141 , GRCh37.p13 chr9: 73,024,057-73,024,057 KLF9
    nsv6178110copy number variation1nstd214human GRCh38 chr9: 70,409,104-70,409,197 , GRCh37.p13 chr9: 73,024,020-73,024,113 KLF9
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