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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055573inversion1nstd229human GRCh38 chr5: 24,120,786-24,120,896 , GRCh37.p13 chr5: 24,120,895-24,121,005 LINC02899
    nsv7055132inversion1nstd229human GRCh38 chr5: 23,968,752-23,975,848 , GRCh37.p13 chr5: 23,968,861-23,975,957 LINC02899
    nsv7053321inversion1nstd229human GRCh38 chr5: 23,205,487-23,975,843 , GRCh37.p13 chr5: 23,205,596-23,975,952 PTPN11P4, LINC02899, 4 more genes
    nsv7052013inversion1nstd229human GRCh38 chr5: 24,052,377-24,052,414 , GRCh37.p13 chr5: 24,052,486-24,052,523 LINC02899
    nsv7047284inversion1nstd229human GRCh38 chr5: 18,365,039-24,500,882 , GRCh37.p13 chr5: 18,365,148-24,500,991 LOC105374683, SNORA105A, 40 more genes
    nsv7047140inversion1nstd229human GRCh38 chr5: 21,512,061-29,406,624 , GRCh37.p13 chr5: 21,512,170-29,406,731 AKTIPP2, RNU4-43P, 48 more genes
    nsv7045172inversion1nstd229human GRCh38 chr5: 18,376,939-24,500,874 , GRCh37.p13 chr5: 18,377,048-24,500,983 LOC102723561, LOC100420804, 40 more genes
    nsv7039059inversion1nstd229human GRCh38 chr5: 24,064,265-24,064,417 , GRCh37.p13 chr5: 24,064,374-24,064,526 LINC02899
    nsv7038908inversion1nstd229human GRCh38 chr5: 24,106,073-24,106,129 , GRCh37.p13 chr5: 24,106,182-24,106,238 LINC02899
    nsv6777714copy number variation1nstd229human GRCh38 chr5: 24,050,145-24,104,800 , GRCh37.p13 chr5: 24,050,254-24,104,909 LINC02899
    nsv6777240copy number variation1nstd229human GRCh38 chr5: 24,166,108-24,166,272 , GRCh37.p13 chr5: 24,166,217-24,166,381 LINC02899
    nsv6777043copy number variation1nstd229human GRCh38 chr5: 24,092,553-24,105,526 , GRCh37.p13 chr5: 24,092,662-24,105,635 LINC02899
    nsv6775293copy number variation1nstd229human GRCh38 chr5: 24,138,501-24,141,800 , GRCh37.p13 chr5: 24,138,610-24,141,909 LINC02899
    nsv6774443copy number variation1nstd229human GRCh38 chr5: 24,027,898-24,028,009 , GRCh37.p13 chr5: 24,028,007-24,028,118 LINC02899
    nsv6773739copy number variation1nstd229human GRCh38 chr5: 24,085,732-24,086,091 , GRCh37.p13 chr5: 24,085,841-24,086,200 LINC02899
    nsv6773299copy number variation1nstd229human GRCh38 chr5: 24,029,830-24,066,310 , GRCh37.p13 chr5: 24,029,939-24,066,419 LINC02899
    nsv6772895copy number variation1nstd229human GRCh38 chr5: 23,966,307-23,966,506 , GRCh37.p13 chr5: 23,966,416-23,966,615 LINC02899
    nsv6772781copy number variation1nstd229human GRCh38 chr5: 24,044,092-24,235,656 , GRCh37.p13 chr5: 24,044,201-24,235,765 LOC503540, LINC02899, 1 more genes
    nsv6771081copy number variation1nstd229human GRCh38 chr5: 24,022,101-24,061,800 , GRCh37.p13 chr5: 24,022,210-24,061,909 LINC02899
    nsv6771028copy number variation1nstd229human GRCh38 chr5: 24,049,965-24,059,126 , GRCh37.p13 chr5: 24,050,074-24,059,235 LINC02899
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