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Items: 1 to 20 of 211

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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
    nsv7096005copy number variation1nstd102humanUncertain significance GRCh37 chr1: 7,700,440-8,601,397 , GRCh38.p12 chr1: 7,640,380-8,541,338 RNU1-7P, PER3, 18 more genes
    nsv7095540copy number variation1nstd102humanPathogenic GRCh37 chr1: 8,022,846-8,037,818 , GRCh38.p12 chr1: 7,962,786-7,977,758 PARK7
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 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
    nsv7050952inversion1nstd229human GRCh38 chr1: 7,187,356-8,831,900 , GRCh37.p13 chr1: 7,247,416-8,891,959 RPL7P7, LOC107984915, 26 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
    nsv7044144inversion1nstd229human GRCh38 chr1: 6,762,728-10,175,549 , GRCh37.p13 chr1: 6,822,788-10,235,607 RPL7P11, LOC105376691, 68 more genes
    nsv6655520copy number variation1nstd229human GRCh38 chr1: 7,958,434-7,976,998 , GRCh37.p13 chr1: 8,018,494-8,037,058 PARK7
    nsv6655519copy number variation1nstd229human GRCh38 chr1: 7,957,581-7,963,593 , GRCh37.p13 chr1: 8,017,641-8,023,653 PARK7
    nsv6655286copy number variation1nstd229human GRCh38 chr1: 7,966,301-7,968,600 , GRCh37.p13 chr1: 8,026,361-8,028,660 PARK7
    nsv6654757copy number variation1nstd229human GRCh38 chr1: 7,985,283-7,985,401 , GRCh37.p13 chr1: 8,045,343-8,045,461 PARK7
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6636971copy number variation1nstd102humanPathogenic GRCh37 chr1: 7,526,232-8,290,521 , GRCh38.p12 chr1: 7,466,172-8,230,461 TNFRSF9, LINC01714, 13 more genes
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 GPR157, MST1L, 313 more genes
    nsv6551355inversion1nstd223human GRCh38 chr1: 7,968,257-7,968,966 , GRCh37.p13 chr1: 8,028,317-8,029,026 PARK7
    nsv6546482inversion1nstd223human GRCh38 chr1: 7,187,356-8,831,900 , GRCh37.p13 chr1: 7,247,416-8,891,959 RERE, RNU1-7P, 26 more genes
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