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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098987copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 97,873,920-97,887,367 , GRCh38.p12 chr9: 95,111,638-95,125,085 FANCC, AOPEP, 1 more genes
    nsv7077729inversion1nstd229human GRCh38 chr9: 94,417,509-96,970,614 , GRCh37.p13 chr9: 97,179,791-99,732,896 HSD17B3-AS1, ERCC6L2, 60 more genes
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv7065950inversion1nstd229human GRCh38 chr9: 95,084,728-95,254,679 , GRCh37.p13 chr9: 97,847,010-98,016,961 AOPEP, MIR24-1, 7 more genes
    nsv7061823inversion1nstd229human GRCh38 chr9: 94,710,575-96,645,135 , GRCh37.p13 chr9: 97,472,857-99,407,417 LOC105376163, LINC00092, 42 more genes
    nsv6872628copy number variation1nstd229human GRCh38 chr9: 94,768,901-95,577,300 , GRCh37.p13 chr9: 97,531,183-98,339,582 RPS26P37, MIR27B, 17 more genes
    nsv6637944copy number variation1nstd102humanPathogenic GRCh37 chr9: 95,711,603-98,469,214 , GRCh38.p12 chr9: 92,949,321-95,706,932 MIRLET7D, MIR24-1, 60 more genes
    nsv6635993copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr9: 95,111,638-95,240,648 , GRCh37 chr9: 97,873,920-98,002,930 FANCC, AOPEP, 2 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
    nsv6447755copy number variation1nstd223human GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516 EIF4BP3, VN1R51P, 162 more genes
    nsv6447347copy number variation1nstd223human GRCh38 chr9: 95,084,456-95,130,122 , GRCh37.p13 chr9: 97,846,738-97,892,404 FANCC, AOPEP, 6 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
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 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
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6313295copy number variation1nstd102humanUncertain significance GRCh37 chr9: 97,365,663-99,064,386 , GRCh38.p12 chr9: 94,603,381-96,302,104 EIF4BP3, MIR2278, 37 more genes
    nsv6313118copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr9: 95,114,619-95,172,157 , GRCh37 chr9: 97,876,901-97,934,439 FANCC, AOPEP, 2 more genes
    nsv6313117copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,863,979-97,934,439 , GRCh38.p12 chr9: 95,101,697-95,172,157 FANCC, RNA5SP288, 3 more genes
    nsv6290855copy number variation1nstd102humanUncertain significance GRCh37 chr9: 97,678,918-98,785,455 , GRCh38.p12 chr9: 94,916,636-96,023,173 MIR6081, LOC105376155, 26 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
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