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 163

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098920copy number variation1nstd102humanUncertain significance GRCh38 chr9: 99,779,833-99,839,574 , GRCh37.p13 chr9: 102,542,115-102,601,856 LOC101928438, NR4A3
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv6871788copy number variation1nstd229human GRCh38 chr9: 99,775,201-99,846,600 , GRCh37.p13 chr9: 102,537,483-102,608,882 LOC101928438, NR4A3
    nsv6858696copy number variation1nstd229human GRCh38 chr9: 99,852,206-99,862,338 , GRCh37.p13 chr9: 102,614,488-102,624,620 NR4A3
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6453422copy number variation1nstd223human GRCh38 chr9: 99,812,401-99,835,400 , GRCh37.p13 chr9: 102,574,683-102,597,682 NR4A3, LOC101928438
    nsv6447755copy number variation1nstd223human GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516 EIF4BP3, VN1R51P, 162 more genes
    nsv6439888copy number variation1nstd223human GRCh38 chr9: 99,814,301-99,821,900 , GRCh37.p13 chr9: 102,576,583-102,584,182 NR4A3, LOC101928438
    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
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 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
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6312742copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 100,190,748-103,062,956 , GRCh38.p12 chr9: 97,428,466-100,300,674 FOXE1, LOC107987011, 47 more genes
    nsv6294493mobile element insertion1nstd186human GRCh37 chr9: 102,626,545-102,626,596 , GRCh38.p12 chr9: 99,864,263-99,864,314 NR4A3
    nsv6136089copy number variation1nstd213human GRCh37 chr9: 100,650,000-102,930,001 , GRCh38.p12 chr9: 97,887,718-100,167,719 TGFBR1, NR4A3, 36 more genes
    nsv6098342insertion1nstd212human GRCh38 chr9: 99,855,556-99,855,556 , GRCh37.p13 chr9: 102,617,838-102,617,838 NR4A3
    nsv5965927insertion1nstd209human GRCh38 chr9: 99,862,549-99,862,549 , GRCh37.p13 chr9: 102,624,831-102,624,831 NR4A3
    nsv5918920copy number variation1nstd209human GRCh38 chr9: 99,828,561-99,828,680 , GRCh37.p13 chr9: 102,590,843-102,590,962 NR4A3
    nsv5909472copy number variation1nstd209human GRCh38 chr9: 99,862,498-99,862,580 , GRCh37.p13 chr9: 102,624,780-102,624,862 NR4A3
    nsv5723608mobile element insertion1nstd211human GRCh38 chr9: 99,850,048-99,850,048 , GRCh37.p13 chr9: 102,612,330-102,612,330 NR4A3
    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