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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051968inversion1nstd229human GRCh38 chr3: 56,944,702-65,952,705 , GRCh37.p13 chr3: 56,978,730-65,938,380 ILF2P1, ARHGEF3-AS1, 115 more genes
    nsv7048271inversion1nstd229human GRCh38 chr3: 59,959,176-65,947,271 , GRCh37.p13 chr3: 59,944,902-65,932,946 LOC105377124, RPS10P10, 63 more genes
    nsv7039673inversion1nstd229human GRCh38 chr3: 59,959,184-65,957,254 , GRCh37.p13 chr3: 59,944,910-65,942,929 PPIAP70, LOC105377114, 63 more genes
    nsv6710496copy number variation1nstd229human GRCh38 chr3: 64,008,254-64,008,334 , GRCh37.p13 chr3: 63,993,930-63,994,010 PSMD6-AS2
    nsv6709889copy number variation1nstd229human GRCh38 chr3: 64,010,532-64,010,590 , GRCh37.p13 chr3: 63,996,208-63,996,266 PSMD6, PSMD6-AS2
    nsv6290933copy number variation1nstd102humanPathogenic GRCh37 chr3: 59,332,508-70,686,155 , GRCh38.p12 chr3: 59,346,782-70,637,004 NDUFB4P1, UBA3, 110 more genes
    nsv6134821copy number variation1nstd213human GRCh37 chr3: 63,570,000-64,090,001 , GRCh38.p12 chr3: 63,584,324-64,104,325 ATXN7, PSMD6, 14 more genes
    nsv6134701copy number variation1nstd213human GRCh37 chr3: 63,610,000-66,170,001 , GRCh38.p12 chr3: 63,624,324-66,184,326 ATXN7, MAGI1, 36 more genes
    nsv6134696copy number variation1nstd213human GRCh37 chr3: 60,070,000-66,170,001 , GRCh38.p12 chr3: 60,084,274-66,184,326 FHIT, PTPRG, 65 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4918615copy number variation1nstd200human GRCh38 chr3: 64,008,296-64,008,489 , GRCh37.p13 chr3: 63,993,972-63,994,165 PSMD6-AS2
    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
    nsv4674306copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,449,667-65,561,638 , GRCh38.p12 chr3: 60,463,934-65,575,963 THOC7-AS1, LOC105377647, 56 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
    nsv4452524copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,076,136-65,716,956 , GRCh38.p12 chr3: 57,042,108-65,731,281 LOC105377114, FAM107A, 110 more genes
    nsv3922383copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,956,521-68,514,983 , NCBI36 chr3: 61,931,561-68,597,673 , GRCh38 chr3: 61,970,847-68,465,832 UBL5P3, PRICKLE2-DT, 73 more genes
    nsv3920449copy number variation1nstd102humanUncertain significance GRCh38 chr3: 63,822,831-64,433,817 , NCBI36 chr3: 63,783,547-64,394,533 , GRCh37 chr3: 63,808,507-64,419,493 ATXN7, THOC7, 12 more genes
    nsv3919181copy number variation1nstd102humanPathogenic GRCh38 chr3: 54,045,018-66,060,461 , GRCh37 chr3: 54,079,045-66,046,136 , NCBI36 chr3: 54,054,085-66,021,176 MAGI1-AS1, FEZF2, 135 more genes
    nsv3917204copy number variation1nstd102humanPathogenic GRCh38 chr3: 57,430,538-64,884,522 , NCBI36 chr3: 57,391,305-64,845,237 , GRCh37 chr3: 57,416,265-64,870,197 C3orf49, PPIAP16, 93 more genes
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