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Items: 1 to 20 of 214

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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
    nsv6876694copy number variation1nstd229human GRCh38 chr9: 96,027,637-96,103,276 , GRCh37.p13 chr9: 98,789,919-98,865,558 LOC158435, ERCC6L2, 1 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
    nsv6871714copy number variation1nstd229human GRCh38 chr9: 96,067,101-96,070,300 , GRCh37.p13 chr9: 98,829,383-98,832,582 LOC158435
    nsv6863866copy number variation1nstd229human GRCh38 chr9: 96,051,524-96,113,341 , GRCh37.p13 chr9: 98,813,806-98,875,623 LOC158434, LOC158435
    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
    nsv6858596copy number variation1nstd229human GRCh38 chr9: 96,087,864-96,088,495 , GRCh37.p13 chr9: 98,850,146-98,850,777 LOC158435
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6448829copy number variation1nstd223human GRCh38 chr9: 96,087,887-96,088,894 , GRCh37.p13 chr9: 98,850,169-98,851,176 LOC158435
    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
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6182795copy number variation1nstd214human GRCh38 chr9: 96,083,171-96,083,302 , GRCh37.p13 chr9: 98,845,453-98,845,584 LOC158435
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