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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
    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
    nsv7061823inversion1nstd229human GRCh38 chr9: 94,710,575-96,645,135 , GRCh37.p13 chr9: 97,472,857-99,407,417 LOC105376163, LINC00092, 42 more genes
    nsv6875818copy number variation1nstd229human GRCh38 chr9: 95,688,189-96,229,236 , GRCh37.p13 chr9: 98,450,471-98,991,518 LOC107987103, LINC00092, 12 more genes
    nsv6865151copy number variation1nstd229human GRCh38 chr9: 96,013,501-96,023,000 , GRCh37.p13 chr9: 98,775,783-98,785,282 LINC00092, LOC105376159, 1 more genes
    nsv6860707copy number variation1nstd229human GRCh38 chr9: 95,873,000-96,070,703 , GRCh37.p13 chr9: 98,635,282-98,832,985 ERCC6L2, ERCC6L2-AS1, 5 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
    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
    nsv6313298copy number variation1nstd102humanUncertain significance GRCh37 chr9: 98,638,288-99,008,892 , GRCh38.p12 chr9: 95,876,006-96,246,610 HSD17B3-AS1, RNA5SP289, 11 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
    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
    nsv6136852copy number variation1nstd213human GRCh37 chr9: 98,740,000-99,490,001 , GRCh38.p12 chr9: 95,977,718-96,727,719 CDC14B, HABP4, 17 more genes
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4676103copy number variation1nstd102humanPathogenic NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211 MIR3074, LOC112268039, 108 more genes
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