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
    nsv7148095copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,341,598-124,103,434 , GRCh38.p12 chr12: 120,903,795-123,618,887 ANAPC5, MLXIP, 82 more genes
    nsv7138072copy number variation1nstd232human GRCh37.p13 chr12: 122,608,885-122,608,960 , GRCh38.p12 chr12: 122,124,338-122,124,413 , GRCh38.p12 chr12|NW_011332697.1: 65,295-65,370 MLXIP
    nsv7094203copy number variation1nstd102humanUncertain significance GRCh37 chr12: 122,277,634-124,242,579 , GRCh38.p12 chr12: 121,839,728-123,758,032 SBNO1, MIR9902-1, 58 more genes
    nsv7059890inversion1nstd229human GRCh38 chr12: 122,105,225-122,114,442 , GRCh37.p13 chr12: 122,589,772-122,598,989 MLXIP
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6932783copy number variation1nstd229human GRCh38 chr12: 122,131,089-122,138,284 , GRCh37.p13 chr12: 122,615,636-122,622,831 MLXIP
    nsv6922730copy number variation1nstd229human GRCh38 chr12: 122,117,558-122,125,988 , GRCh37.p13 chr12: 122,602,105-122,610,535 MLXIP
    nsv6920920copy number variation1nstd229human GRCh38 chr12: 121,001,001-122,266,400 , GRCh37.p13 chr12: 121,438,804-122,750,947 BCL7A, KDM2B, 36 more genes
    nsv6919929copy number variation1nstd229human GRCh38 chr12: 122,098,010-122,110,516 , GRCh37.p13 chr12: 122,582,557-122,595,063 MLXIP
    nsv6919601copy number variation1nstd229human GRCh38 chr12: 122,107,448-122,190,892 , GRCh37.p13 chr12: 122,591,995-122,675,439 IL31, LRRC43, 1 more genes
    nsv6584223inversion1nstd223human GRCh38 chr12: 122,119,130-122,119,658 , GRCh37.p13 chr12: 122,603,677-122,604,205 MLXIP
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6484688copy number variation1nstd223human GRCh38 chr12: 122,097,197-122,101,606 , GRCh37.p13 chr12: 122,581,744-122,586,153 MLXIP
    nsv6483480copy number variation1nstd223human GRCh38 chr12: 122,119,624-122,121,167 , GRCh37.p13 chr12: 122,604,171-122,605,714 MLXIP
    nsv6479612copy number variation1nstd223human GRCh38 chr12: 122,076,801-122,080,300 , GRCh37.p13 chr12: 122,514,707-122,518,206 MLXIP
    nsv6290266copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,887,337-123,386,068 , GRCh38.p12 chr12: 121,449,534-122,901,521 LINC02985, DENR, 38 more genes
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6274124copy number variation1nstd214human GRCh38 chr12: 122,093,878-122,093,951 , GRCh37.p13 chr: NaN-NaN MLXIP
    nsv6273802copy number variation1nstd214human GRCh38 chr12: 122,124,193-122,124,294 , GRCh37.p13 chr12: 122,608,740-122,608,841 MLXIP
    nsv6271433copy number variation1nstd214human GRCh38 chr12: 122,124,338-122,124,413 , GRCh37.p13 chr12: 122,608,885-122,608,960 MLXIP
    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