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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072956inversion1nstd229human GRCh38 chr12: 49,906,455-49,909,257 , GRCh37.p13 chr12: 50,300,238-50,303,040 LINC02396
    nsv6926225copy number variation1nstd229human GRCh38 chr12: 49,806,728-50,041,233 , GRCh37.p13 chr12: 50,200,511-50,435,016 RACGAP1, AQP5, 13 more genes
    nsv6467945copy number variation1nstd223human GRCh38 chr12: 49,905,309-49,906,913 , GRCh37.p13 chr12: 50,299,092-50,300,696 LINC02396
    nsv6288546insertion1nstd214human GRCh38 chr12: 49,908,108-49,908,108 , GRCh37.p13 chr12: 50,301,891-50,301,891 LINC02396
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132250copy number variation1nstd213human GRCh37 chr12: 49,440,000-51,850,001 , GRCh38.p12 chr12: 49,046,217-51,456,217 DAZAP2, KCNH3, 83 more genes
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4601871copy number variation1nstd183human GRCh37 chr12: 50,302,685-50,305,898 , GRCh38.p12 chr12: 49,908,902-49,912,115 LINC02395, LINC02396
    nsv4601410copy number variation1nstd183human GRCh37 chr12: 50,304,926-50,306,973 , GRCh38.p12 chr12: 49,911,143-49,913,190 LINC02396, LINC02395
    nsv4385013copy number variation1nstd173human GRCh37 chr12: 50,199,651-50,434,014 , GRCh38.p12 chr12: 49,805,868-50,040,231 , FAIM2, 14 more genes
    nsv4376507copy number variation2nstd173human GRCh37 chr12: 50,199,682-50,434,033 , GRCh38.p12 chr12: 49,805,899-50,040,250 , BCDIN3D-AS1, 14 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv3922260copy number variation1nstd102humanUncertain significance NCBI36 chr12: 48,520,125-48,995,258 , GRCh38 chr12: 49,840,075-50,315,208 , GRCh37 chr12: 50,233,858-50,708,991 CERS5, LINC02395, 21 more genes
    nsv3920847inversion1nstd102humanUncertain significance GRCh38.p12 chr12: 26,217,318-53,967,754 , GRCh37 chr12: 26,370,251-54,361,538 , ASIC1, 491 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 , BTG1P1, 2451 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 , OR5BT1P, 2441 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 , RNA5SP369, 2454 more genes
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