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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5574655copy number variation1nstd207human GRCh38 chr3: 75,653,537-75,653,592 , GRCh37.p13 chr3: 75,702,688-75,702,743 AGGF1P3, FRG2C
    nsv5439187copy number variation1nstd206human GRCh38 chr3: 75,443,163-75,861,638 , GRCh37.p13 chr3: 75,492,314-75,910,789 , RPS3AP15, 16 more genes
    nsv5033386inversion1nstd200human GRCh38 chr3: 66,830,019-82,426,887 , GRCh37.p13 chr3: 66,880,443-82,476,038 , HNRNPA3P6, 150 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4713275copy number variation1nstd195human GRCh37 chr3: 75,688,951-75,756,701 , GRCh38.p12 chr3: 75,639,800-75,707,550 AGGF1P3, LINC00960, 3 more genes
    nsv4710693copy number variation1nstd195human GRCh37 chr3: 75,688,901-75,701,201 , GRCh38.p12 chr3: 75,639,750-75,652,050 AGGF1P3, FRG2C
    nsv4708845copy number variation1nstd195human GRCh37 chr3: 75,688,901-75,756,651 , GRCh38.p12 chr3: 75,639,750-75,707,500 AGGF1P3, LINC00960, 3 more genes
    nsv4705391copy number variation1nstd195human GRCh37 chr3: 75,701,251-75,715,901 , GRCh38.p12 chr3: 75,652,100-75,666,750 AGGF1P3, RARRES2P1, 1 more genes
    nsv4701727copy number variation1nstd195human GRCh37 chr3: 75,688,901-75,756,601 , GRCh38.p12 chr3: 75,639,750-75,707,450 AGGF1P3, LINC00960, 3 more genes
    nsv4674621copy number variation1nstd102humanUncertain significance GRCh37 chr3: 75,200,750-76,084,525 , GRCh38.p12 chr3: 75,151,599-76,035,374 SNRPCP10, LINC02018, 26 more genes
    nsv4674351copy number variation1nstd102humanUncertain significance GRCh37 chr3: 75,404,228-76,636,256 , GRCh38.p12 chr3: 75,355,077-76,587,105 CLUHP10, LINC02018, 22 more genes
    nsv4596628copy number variation1nstd183human GRCh37 chr3: 75,700,163-75,704,178 , GRCh38.p12 chr3: 75,651,012-75,655,027 AGGF1P3, FRG2C
    nsv4589016copy number variation1nstd183human GRCh37 chr3: 75,576,888-75,832,561 , GRCh38.p12 chr3: 75,527,737-75,783,410 , LINC00960, 13 more genes
    nsv4586694copy number variation1nstd183human GRCh37 chr3: 75,567,240-75,817,199 , GRCh38.p12 chr3: 75,518,089-75,768,048 , OR7E121P, 14 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4407467copy number variation1nstd174human GRCh37 chr3: 75,626,829-75,765,976 , GRCh38.p12 chr3: 75,577,678-75,716,825 UNC93B3, FRG2C, 9 more genes
    nsv4403857copy number variation1nstd174human GRCh37 chr3: 75,396,818-75,918,869 , GRCh38.p12 chr3: 75,347,667-75,869,718 , OR7E55P, 22 more genes
    nsv4397456copy number variation1nstd174human GRCh37 chr3: 75,695,517-75,809,258 , GRCh38.p12 chr3: 75,646,366-75,760,107 AGGF1P3, LINC00960, 6 more genes
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