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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6454958copy number variation1nstd223human GRCh38 chr9: 41,455,001-41,580,500 , GRCh37.p13 chr9: 45,604,871-45,952,289 RPL7AP45, RN7SL565P, 2 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
    nsv6304912copy number variation1nstd186human GRCh37 chr9: 46,044,395-46,067,906 , GRCh38.p12 chr9: 41,575,126-41,598,637 RN7SL565P
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6142004copy number variation1nstd206human GRCh38 chr9: 41,291,900-41,795,800 , GRCh37.p13 chr9: 45,374,923-47,201,341 , LOC105376065, 10 more genes
    nsv5911060copy number variation1nstd209human GRCh38 chr9: 40,229,279-42,858,473 , GRCh37.p13 chr9: 42,792,885-46,287,854 , LOC107984035, 69 more genes
    nsv5909117copy number variation1nstd209human GRCh38 chr9: 40,903,761-43,206,180 , GRCh37.p13 chr9: 40,029,241-41,240,039 , LOC100420440, 62 more genes
    nsv5664563inversion1nstd207human GRCh38 chr9: 39,265,868-42,796,744 , GRCh37.p13 chr9: 42,792,885-46,287,854 , PTGER4P1, 95 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
    nsv5255031copy number variation1nstd204human GRCh38.p13 chr9: 41,545,101-41,636,200 , GRCh37.p13 chr9: 46,014,370-46,105,469 RN7SL565P
    nsv5250988copy number variation1nstd204human GRCh38.p13 chr9: 41,576,901-41,577,400 , GRCh37.p13 chr9: 46,046,170-46,046,669 RN7SL565P
    nsv5248836copy number variation1nstd204human GRCh38.p13 chr9: 41,365,601-41,607,300 , GRCh37.p13 chr9: 45,448,624-46,076,569 , LOC107984035, 3 more genes
    nsv5248493copy number variation1nstd204human GRCh38.p13 chr9: 41,543,301-41,594,800 , GRCh37.p13 chr9: 46,012,570-46,064,069 RN7SL565P
    nsv5246644copy number variation1nstd204human GRCh38.p13 chr9: 41,563,801-41,582,000 , GRCh37.p13 chr9: 46,033,070-46,051,269 RN7SL565P
    nsv5245832copy number variation1nstd204human GRCh38.p13 chr9: 41,577,401-41,594,700 , GRCh37.p13 chr9: 46,046,670-46,063,969 RN7SL565P
    nsv5245008copy number variation1nstd204human GRCh38.p13 chr9: 41,424,201-41,582,200 , GRCh37.p13 chr9: 45,507,224-46,051,469 LOC105376065, LOC107984035, 2 more genes
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