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Items: 1 to 20 of 399

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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
    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
    nsv6257667mobile element insertion1nstd215human GRCh38 chr9: 62,810,374-62,810,374 , GRCh37.p13 chr9: 66,466,198-66,466,198 LINC01410
    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
    nsv6109908inversion1nstd212human GRCh38 chr9: 62,806,330-62,818,555 , GRCh37.p13 chr9: 66,462,154-66,474,379 LINC01410
    nsv6088505insertion1nstd212human GRCh38 chr9: 62,810,365-62,810,365 , GRCh37.p13 chr9: 66,466,189-66,466,189 LINC01410
    nsv6085574insertion1nstd212human GRCh38 chr9: 62,802,344-62,802,344 , GRCh37.p13 chr9: 66,458,168-66,458,168 RNA5SP283, LINC01410
    nsv6012725copy number variation1nstd212human GRCh38 chr9: 62,803,530-62,803,607 , GRCh37.p13 chr9: 66,459,354-66,459,431 LINC01410
    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
    nsv5728953mobile element insertion1nstd211human GRCh38 chr9: 62,813,904-62,813,904 , GRCh37.p13 chr9: 66,469,728-66,469,728 LINC01410
    nsv5727805mobile element insertion1nstd211human GRCh38 chr9: 62,813,904-62,813,904 , GRCh37.p13 chr9: 66,469,728-66,469,728 LINC01410
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