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Items: 1 to 20 of 524

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070730inversion1nstd229human GRCh38 chr9: 62,058,130-67,204,238 , GRCh37.p13 chr9: 41,204,320-44,676,072 ATP5F1AP10, IGKV1OR9-1, 125 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
    nsv6633538copy number variation2nstd224human GRCh37 chr9: 68,158,106-68,435,907 , GRCh38.p12 chr9: 63,562,372-63,840,173 LINC00537, MYO5BP3, 10 more genes
    nsv6454572copy number variation1nstd223human GRCh38 chr9: 63,783,901-63,862,600 , GRCh37.p13 chr9: 68,379,635-68,458,334 LINC00537, MIR4477B, 3 more genes
    nsv6453900copy number variation1nstd223human GRCh38 chr9: 63,767,901-63,831,600 , GRCh37.p13 chr9: 68,363,635-68,427,334 MIR4477B, LINC00537, 6 more genes
    nsv6453090copy number variation1nstd223human GRCh38 chr9: 63,841,601-63,843,200 , GRCh37.p13 chr9: 68,437,335-68,438,934 FRG1JP
    nsv6448076copy number variation1nstd223human GRCh38 chr9: 63,694,501-63,862,700 , GRCh37.p13 chr9: 68,290,235-68,458,434 DUX4L50, PTGER4P3, 9 more genes
    nsv6446660copy number variation1nstd223human GRCh38 chr9: 63,695,801-63,862,700 , GRCh37.p13 chr9: 68,291,535-68,458,434 LOC100419925, LOC107987021, 9 more genes
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 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
    nsv6314573complex chromosomal rearrangement2nstd102humanUncertain significance GRCh38.p12 chr9: 63,838,723-63,838,723 , GRCh38.p12 chr9: 68,221,094-68,221,094 , GRCh38.p12 chr9: 201,090-201,090 , GRCh38.p12 chr9: 201,106-201,106 , GRCh37 chr9: 68,434,457-68,434,457 , GRCh37 chr9: 70,836,010-70,836,010 , GRCh37 chr9: 201,090-201,090 , GRCh37 chr9: 201,106-201,106 FRG1JP
    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
    nsv6142643copy number variation1nstd206human GRCh38 chr9: 63,833,632-63,918,264 , GRCh37.p13 chr9: 68,429,366-68,513,998 FRG1JP
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv6124369insertion1nstd186human GRCh37 chr9: 68,450,269-68,450,273 , GRCh38.p12 chr9: 63,854,535-63,854,539 FRG1JP
    nsv6080813insertion1nstd212human GRCh38 chr9: 63,838,315-63,838,315 , GRCh37.p13 chr9: 68,434,049-68,434,049 FRG1JP
    nsv6004941copy number variation1nstd212human GRCh38 chr9: 63,852,737-63,853,272 , GRCh37.p13 chr9: 68,448,471-68,449,006 FRG1JP
    nsv5919657copy number variation1nstd209human GRCh38 chr9: 63,835,915-63,836,075 , GRCh37.p13 chr9: 68,431,649-68,431,809 FRG1JP
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