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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072903inversion1nstd229human GRCh38 chr12: 52,038,946-52,043,553 , GRCh37.p13 chr12: 52,432,730-52,437,337 NR4A1
    nsv7070117inversion1nstd229human GRCh38 chr12: 52,039,306-52,042,087 , GRCh37.p13 chr12: 52,433,090-52,435,871 NR4A1
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv7064164inversion1nstd229human GRCh38 chr12: 52,056,726-52,056,909 , GRCh37.p13 chr12: 52,450,510-52,450,693 NR4A1
    nsv6935296copy number variation1nstd229human GRCh38 chr12: 52,041,929-52,054,325 , GRCh37.p13 chr12: 52,435,713-52,448,109 NR4A1, LOC107984510
    nsv6934681copy number variation1nstd229human GRCh38 chr12: 52,042,237-52,042,327 , GRCh37.p13 chr12: 52,436,021-52,436,111 NR4A1
    nsv6933554copy number variation1nstd229human GRCh38 chr12: 52,034,970-52,045,477 , GRCh37.p13 chr12: 52,428,754-52,439,261 NR4A1
    nsv6933291copy number variation1nstd229human GRCh38 chr12: 52,047,891-52,048,332 , GRCh37.p13 chr12: 52,441,675-52,442,116 NR4A1, LOC107984510
    nsv6927112copy number variation1nstd229human GRCh38 chr12: 52,051,568-52,054,325 , GRCh37.p13 chr12: 52,445,352-52,448,109 LOC107984510, NR4A1
    nsv6927042copy number variation1nstd229human GRCh38 chr12: 52,043,889-52,054,340 , GRCh37.p13 chr12: 52,437,673-52,448,124 LOC107984510, NR4A1
    nsv6924731copy number variation1nstd229human GRCh38 chr12: 52,028,289-52,031,671 , GRCh37.p13 chr12: 52,422,073-52,425,455 NR4A1
    nsv6922911copy number variation1nstd229human GRCh38 chr12: 52,059,204-52,321,021 , GRCh37.p13 chr12: 52,452,988-52,714,805 KRT87P, KRT86, 14 more genes
    nsv6586342inversion1nstd223human GRCh38 chr12: 52,039,306-52,042,087 , GRCh37.p13 chr12: 52,433,090-52,435,871 NR4A1
    nsv6463112copy number variation1nstd223human GRCh38 chr12: 52,029,391-52,032,110 , GRCh37.p13 chr12: 52,423,175-52,425,894 NR4A1
    nsv6462229copy number variation1nstd223human GRCh38 chr12: 52,059,204-52,321,021 , GRCh37.p13 chr12: 52,452,988-52,714,805 LINC02874, SMIM41, 14 more genes
    nsv6458702copy number variation1nstd223human GRCh38 chr12: 52,047,799-52,048,365 , GRCh37.p13 chr12: 52,441,583-52,442,149 NR4A1, LOC107984510
    nsv6307594copy number variation1nstd186human GRCh37 chr12: 52,442,140-52,443,334 , GRCh38.p12 chr12: 52,048,356-52,049,550 NR4A1, LOC107984510
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132252copy number variation1nstd213human GRCh37 chr12: 51,940,000-52,650,001 , GRCh38.p12 chr12: 51,546,216-52,256,217 ACVR1B, KRT80, 22 more genes
    nsv5934693copy number variation1nstd209human GRCh38 chr12: 52,047,883-52,048,322 , GRCh37.p13 chr12: 52,441,667-52,442,106 NR4A1, LOC107984510
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