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Items: 1 to 20 of 157

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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
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 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
    nsv7052066inversion1nstd229human GRCh38 chr1: 4,379,650-7,782,927 , GRCh37.p13 chr1: 4,439,710-7,842,987 NPHP4, MIR4252, 46 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
    nsv6655141copy number variation1nstd229human GRCh38 chr1: 7,777,319-7,779,625 , GRCh37.p13 chr1: 7,837,379-7,839,685 VAMP3
    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
    nsv6546482inversion1nstd223human GRCh38 chr1: 7,187,356-8,831,900 , GRCh37.p13 chr1: 7,247,416-8,891,959 RERE, RNU1-7P, 26 more genes
    nsv6315409copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746 VAMP3, CTNNBIP1, 245 more genes
    nsv6315340copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,250,285-7,943,864 , GRCh38.p12 chr1: 6,190,225-7,883,804 ICMT-DT, CAMTA1-DT, 33 more genes
    nsv6315170copy number variation1nstd102humanPathogenic GRCh37 chr1: 834,101-7,930,605 , GRCh38.p12 chr1: 898,721-7,870,545 PRDM16-DT, CAMTA1-AS1, 186 more genes
    nsv6313501copy number variation1nstd102humanUncertain significance GRCh37 chr1: 6,360,146-7,888,730 , GRCh38.p12 chr1: 6,300,086-7,828,670 CAMTA1-DT, RPL37P9, 25 more genes
    nsv6290672copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570 RPL9P11, FAM131C2P, 466 more genes
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