U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 158

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098455copy number variation6nstd102humanUncertain significance GRCh37 chr9: 32,453,279-37,785,041 , GRCh38.p12 chr9: 32,453,281-37,785,044 TRBVAOR9-2, UBAP2, 197 more genes
    nsv7098080copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,453,279-35,068,379 , GRCh38.p12 chr9: 32,453,281-35,068,382 SUGT1P1, RNU7-36P, 110 more genes
    nsv7064530inversion1nstd229human GRCh38 chr9: 32,779,950-32,783,922 , GRCh37.p13 chr9: 32,779,948-32,783,920 TMEM215, LOC105376017
    nsv6868207copy number variation1nstd229human GRCh38 chr9: 32,787,910-32,790,689 , GRCh37.p13 chr9: 32,787,908-32,790,687 TMEM215
    nsv6863779copy number variation1nstd229human GRCh38 chr9: 32,789,401-32,792,200 , GRCh37.p13 chr9: 32,789,399-32,792,198 TMEM215
    nsv6858912copy number variation1nstd229human GRCh38 chr9: 32,772,456-32,991,017 , GRCh37.p13 chr9: 32,772,454-32,991,015 BOLA3P4, TMEM215, 5 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
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6315463copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-35,903,398 , GRCh38.p12 chr9: 203,861-35,903,401 IFNA11P, RNU6-14P, 495 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
    nsv6313892copy number variation1nstd102humanPathogenic GRCh37 chr9: 676,264-33,743,670 , GRCh38.p12 chr9: 676,264-33,743,672 SUGT1P1, FOCAD-AS1, 391 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
    nsv6137461copy number variation1nstd213human GRCh37 chr9: 32,140,000-33,310,001 , GRCh38.p12 chr9: 32,140,002-33,310,003 ACO1, BAG1, 31 more genes
    nsv6137089copy number variation1nstd213human GRCh37 chr9: 32,230,000-34,220,001 , GRCh38.p12 chr9: 32,230,002-34,220,003 ANXA2P2, TRBV21OR9-2, 75 more genes
    nsv6137086copy number variation1nstd213human GRCh37 chr9: 29,710,000-37,450,001 , GRCh38.p12 chr9: 29,710,002-37,450,004 AQP7, BAG1, 210 more genes
    nsv5947922insertion1nstd209human GRCh38 chr9: 32,785,950-32,785,950 , GRCh37.p13 chr9: 32,785,948-32,785,948 TMEM215
    nsv5381740copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,399,559-33,541,225 , GRCh38.p12 chr9: 32,399,561-33,541,227 SMU1, RNU4ATAC15P, 38 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center