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 223

    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
    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
    nsv7071183inversion1nstd229human GRCh38 chr12: 122,804,561-124,735,813 , GRCh37.p13 chr12: 123,289,108-125,220,359 TMED2, GTF2H3, 41 more genes
    nsv7058574inversion1nstd229human GRCh38 chr12: 122,435,128-123,376,948 , GRCh37.p13 chr12: 122,919,675-123,861,495 RNA5SP375, HCAR1, 23 more genes
    nsv6936154copy number variation1nstd229human GRCh38 chr12: 122,924,097-122,928,622 , GRCh37.p13 chr12: 123,408,644-123,413,169 ABCB9
    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
    nsv6933981copy number variation1nstd229human GRCh38 chr12: 122,920,953-122,935,071 , GRCh37.p13 chr12: 123,405,500-123,419,618 ABCB9
    nsv6931925copy number variation1nstd229human GRCh38 chr12: 122,956,016-122,956,815 , GRCh37.p13 chr12: 123,440,563-123,441,362 ABCB9
    nsv6928622copy number variation1nstd229human GRCh38 chr12: 122,897,879-122,961,953 , GRCh37.p13 chr12: 123,382,426-123,446,500 ABCB9
    nsv6927694copy number variation1nstd229human GRCh38 chr12: 122,942,425-122,942,457 , GRCh37.p13 chr12: 123,426,972-123,427,004 ABCB9
    nsv6924408copy number variation1nstd229human GRCh38 chr12: 122,644,242-123,080,927 , GRCh37.p13 chr12: 123,128,789-123,565,474 VPS37B, MIR9902-1, 13 more genes
    nsv6920256copy number variation1nstd229human GRCh38 chr12: 122,969,872-122,974,845 , GRCh37.p13 chr12: 123,454,419-123,459,392 ABCB9, OGFOD2
    nsv6918401copy number variation1nstd229human GRCh38 chr12: 122,953,234-122,954,229 , GRCh37.p13 chr12: 123,437,781-123,438,776 ABCB9
    nsv6621066copy number variation1nstd224human GRCh37 chr12: 123,414,349-123,694,602 , GRCh38.p12 chr12: 122,929,802-123,210,055 MPHOSPH9, ABCB9, 5 more genes
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6495235copy number variation1nstd223human GRCh38 chr12: 122,582,127-122,928,683 , GRCh37.p13 chr12: 123,066,674-123,413,230 MIR9902-2, VPS37B, 9 more genes
    nsv6487172copy number variation1nstd223human GRCh38 chr12: 122,966,538-122,969,206 , GRCh37.p13 chr12: 123,451,085-123,453,753 ABCB9
    nsv6484697copy number variation1nstd223human GRCh38 chr12: 122,953,240-122,954,209 , GRCh37.p13 chr12: 123,437,787-123,438,756 ABCB9
    nsv6478495copy number variation1nstd223human GRCh38 chr12: 122,927,333-122,931,486 , GRCh37.p13 chr12: 123,411,880-123,416,033 ABCB9
    nsv6476153copy number variation1nstd223human GRCh38 chr12: 122,954,648-122,970,439 , GRCh37.p13 chr12: 123,439,195-123,454,986 ABCB9
    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