U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 23

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4769364copy number variation1nstd102humanPathogenic GRCh37 chr12: 46,177,220-46,213,044 , GRCh38.p12 chr12: 45,783,437-45,819,261 ARID2
    nsv6289826copy number variation1nstd102humanPathogenic GRCh37 chr12: 46,125,066-46,230,365 , GRCh38.p12 chr12: 45,731,283-45,836,582 ARID2, LOC105369745
    nsv6309242copy number variation1nstd102humanPathogenic GRCh38 chr12: 45,690,000-45,750,000 , GRCh37.p13 chr12: 46,083,783-46,143,783 ARID2, LINC00938
    nsv6634426copy number variation1nstd102humanPathogenic GRCh37 chr12: 46,230,372-46,233,279 , GRCh38.p12 chr12: 45,836,589-45,839,496 ARID2, LOC105369745
    nsv6314133copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 46,207,100-46,242,644 , GRCh38.p12 chr12: 45,813,317-45,848,861 ARID2, LOC105369745
    nsv4456546copy number variation1nstd102humanPathogenic GRCh37 chr12: 46,079,151-46,258,348 , GRCh38.p12 chr12: 45,685,368-45,864,565 ARID2, LOC105369745, 1 more genes
    nsv5980450copy number variation1nstd102humanPathogenic GRCh37 chr12: 46,150,008-46,321,670 , GRCh38.p12 chr12: 45,756,225-45,927,887 ARID2, SCAF11, 3 more genes
    nsv5980443copy number variation1nstd102humanPathogenic GRCh37 chr12: 46,168,172-46,304,719 , GRCh38.p12 chr12: 45,774,389-45,910,936 ARID2, KNOP1P2, 2 more genes
    nsv3319008copy number variation1nstd45humanPathogenic GRCh38.p12 chr12: 45,729,709-45,908,040 , GRCh37 chr12: 46,123,492-46,301,823 ARID2, KNOP1P2, 2 more genes
    nsv4675187copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 46,141,773-46,375,955 , GRCh38.p12 chr12: 45,747,990-45,982,172 ARID2, SCAF11, 3 more genes
    nsv3921330copy number variation1nstd102humanPathogenic GRCh37 chr12: 41,107,689-46,945,683 , GRCh38 chr12: 40,713,887-46,551,900 , NCBI36 chr12: 39,393,956-45,231,950 ARID2, RACGAP1P1, 61 more genes
    nsv6634445copy number variation1nstd102humanPathogenic GRCh37 chr12: 44,661,149-48,921,204 , GRCh38.p12 chr12: 44,267,366-48,527,421 ARID2, ZNF641, 77 more genes
    nsv3916928copy number variation1nstd102humanPathogenic NCBI36 chr12: 42,194,761-46,386,352 , GRCh37.p13 chr12: 43,908,494-48,100,085 , GRCh38.p12 chr12: 43,514,691-47,706,302 ARID2, RPAP3-DT, 51 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 ARID2, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 ARID2, LOH12CR2, 2452 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 ARID2, RNU4ATAC16P, 2452 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 ARID2, BTG1P1, 2451 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 ARID2, OR5BT1P, 2441 more genes
    nsv1398632copy number variation1nstd102humanPathogenic GRCh37 chr12: 31,886,971-50,360,461 , GRCh38.p12 chr12: 31,734,037-49,966,678 ARID2, TUBB8P5, 252 more genes
    nsv3898591copy number variation1nstd102humanPathogenic GRCh37 chr12: 37,857,750-49,791,459 , GRCh38.p12 chr12: 37,463,948-49,397,676 ARID2, ZNF75BP, 195 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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