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Items: 1 to 20 of 909

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6133384copy number variation1nstd213human GRCh37 chr18: 50,080,000-50,710,001 , GRCh38.p12 chr18: 52,553,630-53,183,631 DCC
    nsv6135009copy number variation1nstd213human GRCh37 chr3: 20,620,000-21,040,001 , GRCh38.p12 chr3: 20,578,508-20,998,509 LOC107986068
    nsv6135715copy number variation1nstd213human GRCh37 chr6: 144,860,000-145,230,001 , GRCh38.p12 chr6: 144,538,864-144,908,865 UTRN
    nsv6133491copy number variation1nstd213human GRCh37 chr1: 105,640,000-106,010,001 , GRCh38.p12 chr1: 105,097,378-105,467,379 CDK4P1
    nsv6133458copy number variation1nstd213human GRCh37 chr18: 64,310,000-64,670,001 , GRCh38.p12 chr18: 66,642,763-67,002,764 RNU6-1037P
    nsv6135270copy number variation1nstd213human GRCh37 chr4: 105,430,000-105,780,001 , GRCh38.p12 chr4: 104,508,843-104,858,844 CXXC4-AS1
    nsv6136385copy number variation1nstd213human GRCh37 chr9: 29,250,000-29,590,001 , GRCh38.p12 chr9: 29,250,002-29,590,003 PDK1P1
    nsv6135940copy number variation1nstd213human GRCh37 chr6: 92,770,000-93,110,001 , GRCh38.p12 chr6: 92,060,282-92,400,283 LOC107986625
    nsv6135273copy number variation1nstd213human GRCh37 chr4: 111,950,000-112,290,001 , GRCh38.p12 chr4: 111,028,844-111,368,845 RNU6-289P
    nsv6132996copy number variation1nstd213human GRCh37 chr16: 6,280,000-6,620,001 , GRCh38.p12 chr16: 6,229,999-6,570,000 RBFOX1
    nsv6136344copy number variation1nstd213human GRCh37 chr9: 10,300,000-10,610,001 , GRCh38.p12 chr9: 10,300,000-10,610,001 PTPRD
    nsv6133654copy number variation1nstd213human GRCh37 chr1: 30,030,000-30,340,001 , GRCh38.p12 chr1: 29,557,153-29,867,154 LOC107984934
    nsv6135725copy number variation1nstd213human GRCh37 chr6: 157,260,000-157,690,001 , GRCh38.p12 chr6: 156,938,866-157,238,333 ARID1B
    nsv6134429copy number variation1nstd213human GRCh37 chr2: 154,850,000-155,130,001 , GRCh38.p12 chr2: 153,993,487-154,273,488 GALNT13
    nsv6134824copy number variation1nstd213human GRCh37 chr3: 15,940,000-16,200,001 , GRCh38.p12 chr3: 15,898,493-16,158,494 LOC107986064
    nsv6134152copy number variation1nstd213human GRCh37 chr2: 144,070,000-144,330,001 , GRCh38.p12 chr2: 143,312,431-143,572,432 ARHGAP15
    nsv6133202copy number variation1nstd213human GRCh37 chr16: 5,910,000-6,170,001 , GRCh38.p12 chr16: 5,859,999-6,120,000 RBFOX1
    nsv6135519copy number variation1nstd213human GRCh37 chr6: 69,840,000-70,090,001 , GRCh38.p12 chr6: 69,130,108-69,380,109 ADGRB3
    nsv6135354copy number variation1nstd213human GRCh37 chr4: 67,800,000-68,050,001 , GRCh38.p12 chr4: 66,934,282-67,184,283 LOC105377262
    nsv6134710copy number variation1nstd213human GRCh37 chr3: 74,390,000-74,640,001 , GRCh38.p12 chr3: 74,340,849-74,590,850 CNTN3
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