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Items: 1 to 20 of 469

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5950588insertion1nstd209human GRCh38 chr2: 25,849,064-25,849,064 , GRCh37.p13 chr2: 26,071,933-26,071,933 ASXL2
    nsv5885834copy number variation1nstd209human GRCh38 chr2: 25,773,618-25,774,557 , GRCh37.p13 chr2: 25,996,487-25,997,426 ASXL2
    nsv5868761copy number variation1nstd209human GRCh38 chr2: 25,780,887-25,781,585 , GRCh37.p13 chr2: 26,003,756-26,004,454 ASXL2
    nsv5832848copy number variation1nstd209human GRCh38 chr2: 25,863,289-25,865,538 , GRCh37.p13 chr2: 26,086,158-26,088,407 ASXL2
    nsv5726152mobile element insertion1nstd211human GRCh38 chr2: 25,859,911-25,859,911 , GRCh37.p13 chr2: 26,082,780-26,082,780 ASXL2
    nsv5715495mobile element insertion1nstd211human GRCh38 chr2: 25,791,960-25,791,960 , GRCh37.p13 chr2: 26,014,829-26,014,829 ASXL2
    nsv5689252mobile element insertion1nstd211human GRCh38 chr2: 25,755,316-25,755,316 , GRCh37.p13 chr2: 25,978,185-25,978,185 ASXL2
    nsv5687981mobile element insertion2nstd211human GRCh38 chr2: 25,789,279-25,789,279 , GRCh37.p13 chr2: 26,012,148-26,012,148 ASXL2
    nsv5685056mobile element insertion2nstd211human GRCh38 chr2: 25,765,688-25,765,688 , GRCh37.p13 chr2: 25,988,557-25,988,557 ASXL2
    nsv5675357mobile element insertion1nstd211human GRCh38 chr2: 25,795,950-25,795,950 , GRCh37.p13 chr2: 26,018,819-26,018,819 ASXL2
    nsv5543531insertion1nstd206human GRCh38 chr2: 25,808,055-25,808,073 , GRCh37.p13 chr2: 26,030,924-26,030,942 ASXL2, TPM3P7
    nsv5453320copy number variation1nstd206human GRCh38 chr2: 25,860,227-25,863,354 , GRCh37.p13 chr2: 26,083,096-26,086,223 ASXL2
    nsv5452079copy number variation1nstd206human GRCh38 chr2: 25,848,388-25,849,166 , GRCh37.p13 chr2: 26,071,257-26,072,035 ASXL2
    nsv5451624copy number variation1nstd206human GRCh38 chr2: 25,863,588-25,869,251 , GRCh37.p13 chr2: 26,086,457-26,092,120 ASXL2
    nsv5443316copy number variation1nstd206human GRCh38 chr2: 25,783,871-25,797,270 , GRCh37.p13 chr2: 26,006,740-26,020,139 ASXL2
    nsv5440335copy number variation1nstd206human GRCh38 chr2: 25,773,618-25,774,576 , GRCh37.p13 chr2: 25,996,487-25,997,445 ASXL2
    nsv5438498copy number variation1nstd206human GRCh38 chr2: 25,815,007-25,815,066 , GRCh37.p13 chr2: 26,037,876-26,037,935 ASXL2
    nsv5438185copy number variation1nstd206human GRCh38 chr2: 25,863,114-25,865,459 , GRCh37.p13 chr2: 26,085,983-26,088,328 ASXL2
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