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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147502copy number variation1nstd232human GRCh37.p13 chr3: 15,103,665-15,103,773 , GRCh38.p12 chr3: 15,062,158-15,062,266 MRPS25
    nsv6716998copy number variation1nstd229human GRCh38 chr3: 15,018,201-15,075,400 , GRCh37.p13 chr3: 15,059,708-15,116,907 RBSN, NR2C2, 1 more genes
    nsv6715984copy number variation1nstd229human GRCh38 chr3: 15,044,392-15,065,048 , GRCh37.p13 chr3: 15,085,899-15,106,555 NR2C2, MRPS25
    nsv6712034copy number variation1nstd229human GRCh38 chr3: 14,670,901-15,564,100 , GRCh37.p13 chr3: 14,712,408-15,605,607 COLQ, RNU6-1024P, 22 more genes
    nsv6704270copy number variation1nstd229human GRCh38 chr3: 15,050,501-15,060,800 , GRCh37.p13 chr3: 15,092,008-15,102,307 MRPS25
    nsv6698171copy number variation1nstd229human GRCh38 chr3: 15,061,276-15,064,566 , GRCh37.p13 chr3: 15,102,783-15,106,073 MRPS25
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6374390copy number variation1nstd223human GRCh38 chr3: 15,061,274-15,064,564 , GRCh37.p13 chr3: 15,102,781-15,106,071 MRPS25
    nsv6367237copy number variation1nstd223human GRCh38 chr3: 15,051,489-15,181,815 , GRCh37.p13 chr3: 15,092,996-15,223,322 COL6A4P1, MRPS25, 3 more genes
    nsv6315249copy number variation1nstd102humanPathogenic GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998 RNU6-905P, PRR3P1, 99 more genes
    nsv6291013copy number variation1nstd102humanUncertain significance GRCh37 chr3: 15,085,863-16,402,392 , GRCh38.p12 chr3: 15,044,356-16,360,885 MIR563, RNU6-1024P, 30 more genes
    nsv6161530copy number variation1nstd214human GRCh38 chr3: 15,062,101-15,062,408 , GRCh37.p13 chr3: 15,103,608-15,103,915 MRPS25
    nsv6134411copy number variation1nstd213human GRCh37 chr3: 14,620,000-15,140,001 , GRCh38.p12 chr3: 14,578,493-15,098,494 NR2C2, CCDC174, 9 more genes
    nsv5968065inversion1nstd209human GRCh38 chr3: 14,742,874-15,551,121 , GRCh37.p13 chr3: 14,784,381-15,592,628 , NR2C2, 21 more genes
    nsv5578687copy number variation1nstd207human GRCh38 chr3: 15,062,198-15,062,505 , GRCh37.p13 chr3: 15,103,705-15,104,012 MRPS25
    nsv5446864copy number variation1nstd206human GRCh38 chr3: 15,063,587-15,063,716 , GRCh37.p13 chr3: 15,105,094-15,105,223 MRPS25
    nsv5443202copy number variation1nstd206human GRCh38 chr3: 15,046,819-15,047,014 , GRCh37.p13 chr3: 15,088,326-15,088,521 NR2C2, MRPS25
    nsv5309301copy number variation1nstd204human GRCh38.p13 chr3: 15,051,422-15,058,163 , GRCh37.p13 chr3: 15,092,929-15,099,670 MRPS25
    nsv5216100copy number variation1nstd204human GRCh38.p13 chr3: 15,051,361-15,058,034 , GRCh37.p13 chr3: 15,092,868-15,099,541 MRPS25
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
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