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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5724944mobile element insertion2nstd211human GRCh38 chr1: 100,270,189-100,270,189 , GRCh37.p13 chr1: 100,735,745-100,735,745 RTCA
    nsv5684203mobile element insertion1nstd211human GRCh38 chr1: 100,273,212-100,273,212 , GRCh37.p13 chr1: 100,738,768-100,738,768 RTCA
    nsv5683686mobile element insertion1nstd211human GRCh38 chr1: 100,283,956-100,283,956 , GRCh37.p13 chr1: 100,749,512-100,749,512 RTCA
    nsv5425265copy number variation1nstd206human GRCh38 chr1: 100,283,406-100,284,572 , GRCh37.p13 chr1: 100,748,962-100,750,128 RTCA
    nsv5408777mobile element insertion1nstd206human GRCh38 chr1: 100,273,212-100,273,263 , GRCh37.p13 chr1: 100,738,768-100,738,819 RTCA
    nsv5353656translocation1nstd200human GRCh38 chr1: 100,289,118-100,289,118 , GRCh38 chr1: 100,289,808-100,289,808 , GRCh37.p13 chr1: 100,754,674-100,754,674 , GRCh37.p13 chr1: 100,755,364-100,755,364 RTCA
    nsv5291352copy number variation1nstd204human GRCh38.p13 chr1: 100,289,108-100,289,811 , GRCh37.p13 chr1: 100,754,664-100,755,367 RTCA
    nsv4906383copy number variation1nstd200human GRCh38 chr1: 100,283,455-100,284,523 , GRCh37.p13 chr1: 100,749,011-100,750,079 RTCA
    nsv4906382copy number variation1nstd200human GRCh38 chr1: 100,282,217-100,282,274 , GRCh37.p13 chr1: 100,747,773-100,747,830 RTCA
    nsv4788839copy number variation1nstd200human GRCh37 chr1: 100,754,669-100,755,364 , GRCh38.p12 chr1: 100,289,113-100,289,808 RTCA
    nsv4788838copy number variation1nstd200human GRCh37 chr1: 100,749,011-100,750,080 , GRCh38.p12 chr1: 100,283,455-100,284,524 RTCA
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4745469copy number variation1nstd199human GRCh37 chr1: 86,005,697-146,486,085 , GRCh38.p12 chr1: 85,540,014-149,528,945 , TAF13, 920 more genes
    nsv4679627copy number variation1nstd189human GRCh37.p13 chr1: 100,661,887-101,495,928 , GRCh38.p12 chr1: 100,196,331-101,030,372 DBT, EXTL2, 18 more genes
    nsv4674470copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,704,867-101,205,009 , GRCh38.p12 chr1: 100,239,311-100,739,453 RTCA-AS1, RTCA, 11 more genes
    nsv4593712copy number variation1nstd183human GRCh37 chr1: 100,752,563-100,757,425 , GRCh38.p12 chr1: 100,287,007-100,291,869 RTCA
    nsv4533568insertion1nstd166human GRCh37.p13 chr1: 100,735,731-100,735,731 , GRCh38.p12 chr1: 100,270,175-100,270,175 RTCA
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
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