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 115

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6875526copy number variation1nstd229human GRCh38 chr9: 76,848,946-77,076,276 , GRCh37.p13 chr9: 79,463,862-79,691,192 ATP5MFP3, LOC105376096, 4 more genes
    nsv6870806copy number variation1nstd229human GRCh38 chr9: 76,566,525-77,206,120 , GRCh37.p13 chr9: 79,181,441-79,821,036 LYPLA2P3, PRUNE2, 8 more genes
    nsv6868809copy number variation1nstd229human GRCh38 chr9: 76,957,921-77,024,020 , GRCh37.p13 chr9: 79,572,837-79,638,936 LYPLA2P3, FOXB2
    nsv6863618copy number variation1nstd229human GRCh38 chr9: 77,016,220-77,020,653 , GRCh37.p13 chr9: 79,631,136-79,635,569 FOXB2
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6557715inversion1nstd223human GRCh38 chr9: 75,901,418-82,872,806 , GRCh37.p13 chr9: 78,516,334-85,487,721 , LOC105376096, 79 more genes
    nsv6442132copy number variation1nstd223human GRCh38 chr9: 77,021,201-77,025,400 , GRCh37.p13 chr9: 79,636,117-79,640,316 FOXB2
    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
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 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
    nsv6136396copy number variation1nstd213human GRCh37 chr9: 78,870,000-79,640,001 , GRCh38.p12 chr9: 76,255,084-77,025,085 RFK, RBM22P5, 11 more genes
    nsv4600665copy number variation1nstd183human GRCh37 chr9: 79,246,378-79,721,416 , GRCh38.p12 chr9: 76,631,462-77,106,500 PCA3, PRUNE2, 6 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455928copy number variation1nstd102humanPathogenic GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877 RPL35AP21, LOC105376097, 134 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4455073copy number variation1nstd102humanUncertain significance GRCh37 chr9: 78,672,613-83,349,616 , GRCh38.p12 chr9: 76,057,697-80,734,701 LOC105376100, NPAP1P6, 49 more genes
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 more genes
    nsv4349215copy number variation1nstd102humanPathogenic GRCh37 chr9: 79,520,825-97,201,274 , GRCh38.p12 chr9: 76,905,909-94,438,992 SPATA31C1, LINC02893, 280 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