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 146

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 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
    nsv6450925copy number variation1nstd223human GRCh38 chr9: 99,905,401-99,907,300 , GRCh37.p13 chr9: 102,667,683-102,669,582 STX17-DT, STX17
    nsv6449703copy number variation1nstd223human GRCh38 chr9: 99,906,553-99,908,251 , GRCh37.p13 chr9: 102,668,835-102,670,533 STX17, STX17-DT
    nsv6448446copy number variation1nstd223human GRCh38 chr9: 99,903,601-99,909,100 , GRCh37.p13 chr9: 102,665,883-102,671,382 STX17-DT, STX17
    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
    nsv6439936copy number variation1nstd223human GRCh38 chr9: 99,906,401-99,906,900 , GRCh37.p13 chr9: 102,668,683-102,669,182 STX17-DT, STX17
    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
    nsv6141425copy number variation1nstd206human GRCh38 chr9: 99,900,982-99,903,035 , GRCh37.p13 chr9: 102,663,264-102,665,317 STX17-DT
    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
    nsv6097836insertion1nstd212human GRCh38 chr9: 99,886,900-99,886,900 , GRCh37.p13 chr9: 102,649,182-102,649,182 STX17-DT
    nsv6097066insertion1nstd212human GRCh38 chr9: 99,903,612-99,903,612 , GRCh37.p13 chr9: 102,665,894-102,665,894 STX17-DT
    nsv6003709copy number variation1nstd212human GRCh38 chr9: 99,901,118-99,902,696 , GRCh37.p13 chr9: 102,663,400-102,664,978 STX17-DT
    nsv5909366copy number variation1nstd209human GRCh38 chr9: 99,903,540-99,903,617 , GRCh37.p13 chr9: 102,665,822-102,665,899 STX17-DT
    nsv5706562mobile element insertion1nstd211human GRCh38 chr9: 99,886,910-99,886,910 , GRCh37.p13 chr9: 102,649,192-102,649,192 STX17-DT
    nsv5542944insertion1nstd206human GRCh38 chr9: 99,903,490-99,903,540 , GRCh37.p13 chr9: 102,665,772-102,665,822 STX17-DT
    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