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 239

    loading data ...

    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
    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
    nsv6141573copy number variation1nstd206human GRCh38 chr9: 61,094,000-61,231,887 , GRCh37.p13 chr9: 65,467,759-65,605,646 SPATA31A7, FAM74A4, 2 more genes
    nsv5914346copy number variation1nstd209human GRCh38 chr9: 60,768,680-66,674,368 , GRCh37.p13 chr: NaN-NaN , MEP1AP3, 146 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
    nsv5256259copy number variation1nstd204human GRCh38.p13 chr9: 61,144,601-61,190,200 , GRCh37.p13 chr9: 65,509,446-65,555,045 SPATA31A7, LOC105379249
    nsv5254584copy number variation1nstd204human GRCh38.p13 chr9: 61,176,201-61,197,300 , GRCh37.p13 chr9: 65,502,346-65,523,445 SPATA31A7
    nsv5253746copy number variation1nstd204human GRCh38.p13 chr9: 61,192,501-61,197,300 , GRCh37.p13 chr9: 65,502,346-65,507,145 SPATA31A7
    nsv5253390copy number variation1nstd204human GRCh38.p13 chr9: 61,186,201-61,197,300 , GRCh37.p13 chr9: 65,502,346-65,513,445 SPATA31A7
    nsv5252976copy number variation1nstd204human GRCh38.p13 chr9: 61,189,901-61,194,400 , GRCh37.p13 chr9: 65,505,246-65,509,745 SPATA31A7
    nsv5249416copy number variation1nstd204human GRCh38.p13 chr9: 61,186,401-61,189,800 , GRCh37.p13 chr9: 65,509,846-65,513,245 SPATA31A7
    nsv5249114copy number variation1nstd204human GRCh38.p13 chr9: 61,181,901-61,197,300 , GRCh37.p13 chr9: 65,502,346-65,517,745 SPATA31A7
    nsv5246121copy number variation1nstd204human GRCh38.p13 chr9: 61,139,701-61,189,900 , GRCh37.p13 chr9: 65,509,746-65,559,945 SPATA31A7, LOC105379249
    nsv5245901copy number variation1nstd204human GRCh38.p13 chr9: 61,189,901-61,213,600 , GRCh37.p13 chr9: 65,486,046-65,509,745 FAM74A4, SPATA31A7
    nsv5244690copy number variation1nstd204human GRCh38.p13 chr9: 61,138,701-61,231,700 , GRCh37.p13 chr9: 65,467,946-65,560,945 LOC105379249, FAM74A4, 1 more genes
    nsv5242513copy number variation1nstd204human GRCh38.p13 chr9: 61,174,501-61,190,300 , GRCh37.p13 chr9: 65,509,346-65,525,145 LOC105379249, SPATA31A7
    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