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 248

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075962inversion1nstd229human GRCh38 chr12: 99,728,274-100,301,277 , GRCh37.p13 chr12: 100,122,052-100,695,055 DEPDC4, RN7SL176P, 8 more genes
    nsv7074674inversion1nstd229human GRCh38 chr12: 100,072,817-104,989,567 , GRCh37.p13 chr12: 100,466,595-105,383,345 SYCP3, GOLGA2P5, 84 more genes
    nsv7068612inversion1nstd229human GRCh38 chr12: 100,083,131-104,989,539 , GRCh37.p13 chr12: 100,476,909-105,383,317 EID3, RNU6-1068P, 84 more genes
    nsv6933029copy number variation1nstd229human GRCh38 chr12: 100,269,016-101,400,896 , GRCh37.p13 chr12: 100,662,794-101,794,674 PIGAP1, SCYL2, 10 more genes
    nsv6930973copy number variation1nstd229human GRCh38 chr12: 100,268,934-100,358,348 , GRCh37.p13 chr12: 100,662,712-100,752,126 SCYL2, SLC17A8
    nsv6928813copy number variation1nstd229human GRCh38 chr12: 100,273,935-100,276,896 , GRCh37.p13 chr12: 100,667,713-100,670,674 SCYL2
    nsv6926514copy number variation1nstd229human GRCh38 chr12: 99,947,178-100,328,732 , GRCh37.p13 chr12: 100,340,956-100,722,510 BLTP3B, MIR1827, 8 more genes
    nsv6923699copy number variation1nstd229human GRCh38 chr12: 100,342,056-100,358,886 , GRCh37.p13 chr12: 100,735,834-100,752,664 SLC17A8, SCYL2
    nsv6923067copy number variation1nstd229human GRCh38 chr12: 100,326,101-100,522,200 , GRCh37.p13 chr12: 100,719,879-100,915,978 NR1H4, SLC17A8, 1 more genes
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
    nsv6920185copy number variation1nstd229human GRCh38 chr12: 100,282,181-100,282,482 , GRCh37.p13 chr12: 100,675,959-100,676,260 SCYL2
    nsv6582018inversion1nstd223human GRCh38 chr12: 100,281,809-100,282,017 , GRCh37.p13 chr12: 100,675,587-100,675,795 SCYL2
    nsv6581141inversion1nstd223human GRCh38 chr12: 100,298,655-100,299,179 , GRCh37.p13 chr12: 100,692,433-100,692,957 SCYL2
    nsv6579250inversion1nstd223human GRCh38 chr12: 100,331,104-100,331,371 , GRCh37.p13 chr12: 100,724,882-100,725,149 SCYL2
    nsv6469325copy number variation1nstd223human GRCh38 chr12: 100,333,601-100,335,600 , GRCh37.p13 chr12: 100,727,379-100,729,378 SCYL2
    nsv6459408copy number variation1nstd223human GRCh38 chr12: 100,336,601-100,337,200 , GRCh37.p13 chr12: 100,730,379-100,730,978 SCYL2
    nsv6457143copy number variation1nstd223human GRCh38 chr12: 100,282,181-100,282,482 , GRCh37.p13 chr12: 100,675,959-100,676,260 SCYL2
    nsv6456074copy number variation1nstd223human GRCh38 chr12: 100,264,401-100,270,900 , GRCh37.p13 chr12: 100,658,179-100,664,678 DEPDC4, SCYL2
    nsv6313913copy number variation1nstd102humanUncertain significance GRCh37 chr12: 100,564,593-103,021,075 , GRCh38.p12 chr12: 100,170,815-102,627,297 DEPDC4, SLC5A8, 46 more genes
    nsv6307421copy number variation1nstd186human GRCh37 chr12: 100,675,993-100,676,388 , GRCh38.p12 chr12: 100,282,215-100,282,610 SCYL2
    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