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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
    nsv7066246inversion1nstd229human GRCh38 chr9: 61,567,441-63,740,704 , GRCh37.p13 chr: NaN-NaN FGF7P6, LOC105379807, 47 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
    nsv6439400copy number variation1nstd223human GRCh38 chr9: 62,467,001-62,470,400 , GRCh37.p13 chr9: 46,778,302-46,781,701 FGF7P7, LINC01189
    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
    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
    nsv6142197copy number variation1nstd206human GRCh38 chr9: 62,397,369-62,507,450 , GRCh37.p13 chr9: 46,708,670-46,818,751 LINC01189, FGF7P6, 1 more genes
    nsv6141618copy number variation1nstd206human GRCh38 chr9: 62,497,738-62,678,500 , GRCh37.p13 chr9: 46,809,039-46,989,801 FAM88F, LINC01189, 3 more genes
    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
    nsv5919501copy number variation1nstd209human GRCh38 chr9: 61,557,000-65,487,786 , GRCh37.p13 chr: NaN-NaN , MTCO1P36, 98 more genes
    nsv5918216copy number variation1nstd209human GRCh38 chr9: 61,647,960-65,578,967 , GRCh37.p13 chr: NaN-NaN , SDR42E1P3, 99 more genes
    nsv5914346copy number variation1nstd209human GRCh38 chr9: 60,768,680-66,674,368 , GRCh37.p13 chr: NaN-NaN , MEP1AP3, 146 more genes
    nsv5910323copy number variation1nstd209human GRCh38 chr9: 61,604,972-65,538,433 , GRCh37.p13 chr: NaN-NaN , FAM242E, 98 more genes
    nsv5554508sequence alteration1nstd206human GRCh38 chr9: 39,866,147-63,791,228 , GRCh37.p13 chr9: 39,713,687-67,542,104 , PTGER4P2, 168 more genes
    nsv5260026copy number variation1nstd204human GRCh38.p13 chr9: 62,474,901-62,498,600 , GRCh37.p13 chr9: 46,786,202-46,809,901 LINC01189, FGF7P7
    nsv5260013copy number variation1nstd204human GRCh38.p13 chr9: 62,474,601-62,478,800 , GRCh37.p13 chr9: 46,785,902-46,790,101 FGF7P7, LINC01189
    nsv5259942copy number variation1nstd204human GRCh38.p13 chr9: 62,516,501-62,517,100 , GRCh37.p13 chr9: 46,827,802-46,828,401 LINC01189
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