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Items: 1 to 20 of 137

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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
    nsv6877577copy number variation1nstd229human GRCh38 chr9: 96,755,585-97,161,429 , GRCh37.p13 chr9: 99,517,867-99,923,711 ZNF782, YRDCP2, 15 more genes
    nsv6859639copy number variation1nstd229human GRCh38 chr9: 96,881,267-96,919,742 , GRCh37.p13 chr9: 99,643,549-99,682,024 PTMAP11, LOC107987024, 1 more genes
    nsv6858816copy number variation1nstd229human GRCh38 chr9: 96,909,001-96,921,300 , GRCh37.p13 chr9: 99,671,283-99,683,582 PTMAP11, MFSD14CP, 1 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
    nsv6305767copy number variation1nstd186human GRCh37 chr9: 99,668,834-99,679,057 , GRCh38.p12 chr9: 96,906,552-96,916,775 MFSD14CP, PTMAP11, 1 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
    nsv6142848copy number variation1nstd206human GRCh38 chr9: 96,906,552-96,916,775 , GRCh37.p13 chr9: 99,668,834-99,679,057 MFSD14CP, LOC107987024, 1 more genes
    nsv6142676copy number variation1nstd206human GRCh38 chr9: 96,906,000-96,939,000 , GRCh37.p13 chr9: 99,668,282-99,701,282 MFSD14CP, PTMAP11, 2 more genes
    nsv6136402copy number variation1nstd213human GRCh37 chr9: 99,490,000-99,740,001 , GRCh38.p12 chr9: 96,727,718-96,977,719 ZNF510, MFSD14CP, 7 more genes
    nsv5485310copy number variation1nstd206human GRCh38 chr9: 96,856,726-96,974,338 , GRCh37.p13 chr9: 99,619,008-99,736,620 MFSD14CP, ZNF782, 5 more genes
    nsv5484624copy number variation1nstd206human GRCh38 chr9: 96,908,664-96,922,552 , GRCh37.p13 chr9: 99,670,946-99,684,834 MFSD14CP, PTMAP11, 1 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
    nsv5256795copy number variation1nstd204human GRCh38.p13 chr9: 96,909,282-96,911,432 , GRCh37.p13 chr9: 99,671,564-99,673,714 PTMAP11
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