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Items: 1 to 20 of 255

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099175copy number variation1nstd231human GRCh38.p12 chr1: 6,492,665-9,894,222 , GRCh37 chr1: 6,552,725-9,954,280 RERE, CA6, 70 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7096008copy number variation1nstd102humanUncertain significance GRCh37 chr1: 9,304,994-12,569,078 , GRCh38.p12 chr1: 9,244,935-12,509,024 NMNAT1, DISP3, 91 more genes
    nsv7095543copy number variation1nstd102humanUncertain significance GRCh37 chr1: 9,770,514-11,264,780 , GRCh38.p12 chr1: 9,710,456-11,204,723 DFFA, ANGPTL7, 38 more genes
    nsv7057525inversion1nstd229human GRCh38 chr1: 7,829,944-15,116,659 , GRCh37.p13 chr1: 7,890,004-15,443,155 PEX14, RNU6-304P, 187 more genes
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7052549inversion1nstd229human GRCh38 chr1: 8,322,830-13,737,741 , GRCh37.p13 chr1: 8,382,890-14,064,236 MIR4632, PLOD1, 166 more genes
    nsv7048193inversion1nstd229human GRCh38 chr1: 9,469,567-16,279,388 , GRCh37.p13 chr1: 9,529,626-16,605,883 PRAMEF36P, HNRNPCL3, 193 more genes
    nsv7047983inversion1nstd229human GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655 THAP3, UBIAD1, 165 more genes
    nsv7046461inversion1nstd229human GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517 LINC02606, C1orf127, 165 more genes
    nsv7045919inversion1nstd229human GRCh38 chr1: 9,861,073-9,861,153 , GRCh37.p13 chr1: 9,921,131-9,921,211 CTNNBIP1
    nsv7044144inversion1nstd229human GRCh38 chr1: 6,762,728-10,175,549 , GRCh37.p13 chr1: 6,822,788-10,235,607 RPL7P11, LOC105376691, 68 more genes
    nsv6658046copy number variation1nstd229human GRCh38 chr1: 9,901,485-10,062,847 , GRCh37.p13 chr1: 9,961,543-10,122,905 TMEM274P, RN7SKP269, 8 more genes
    nsv6658043copy number variation1nstd229human GRCh38 chr1: 9,898,201-9,904,900 , GRCh37.p13 chr1: 9,958,259-9,964,958 CTNNBIP1
    nsv6658032copy number variation1nstd229human GRCh38 chr1: 9,855,699-9,859,742 , GRCh37.p13 chr1: 9,915,757-9,919,800 LOC105376717, CTNNBIP1
    nsv6657950copy number variation1nstd229human GRCh38 chr1: 9,875,369-9,882,076 , GRCh37.p13 chr1: 9,935,427-9,942,134 CTNNBIP1
    nsv6657940copy number variation1nstd229human GRCh38 chr1: 9,846,798-9,846,850 , GRCh37.p13 chr1: 9,906,856-9,906,908 CTNNBIP1
    nsv6657919copy number variation1nstd229human GRCh38 chr1: 9,803,781-10,372,657 , GRCh37.p13 chr1: 9,863,839-10,432,715 RN7SL731P, MIR5697, 14 more genes
    nsv6657875copy number variation1nstd229human GRCh38 chr1: 9,881,001-9,887,700 , GRCh37.p13 chr1: 9,941,059-9,947,758 CTNNBIP1
    nsv6657772copy number variation1nstd229human GRCh38 chr1: 9,551,980-10,105,866 , GRCh37.p13 chr1: 9,612,038-10,165,924 SLC25A33, MIR5697, 19 more genes
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