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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6797986copy number variation1nstd229human GRCh38 chr5: 171,803,776-171,812,018 , GRCh37.p13 chr5: 171,230,780-171,239,022 LOC105377725
    nsv6793021copy number variation1nstd229human GRCh38 chr5: 171,807,397-171,812,570 , GRCh37.p13 chr5: 171,234,401-171,239,574 LOC105377725
    nsv6792549copy number variation1nstd229human GRCh38 chr5: 171,825,302-171,825,654 , GRCh37.p13 chr5: 171,252,306-171,252,658 LOC105377725
    nsv6791013copy number variation1nstd229human GRCh38 chr5: 171,817,550-171,823,136 , GRCh37.p13 chr5: 171,244,554-171,250,140 LOC105377725
    nsv6789467copy number variation1nstd229human GRCh38 chr5: 171,830,701-171,898,500 , GRCh37.p13 chr5: 171,257,705-171,325,504 LOC107986476, FBXW11, 1 more genes
    nsv6783955copy number variation1nstd229human GRCh38 chr5: 171,819,976-171,831,848 , GRCh37.p13 chr5: 171,246,980-171,258,852 LOC105377725
    nsv6781511copy number variation1nstd229human GRCh38 chr5: 170,662,244-174,111,903 , GRCh37.p13 chr5: 170,089,248-173,538,906 LOC101928093, LOC107986482, 79 more genes
    nsv6780650copy number variation1nstd229human GRCh38 chr5: 171,733,101-171,829,600 , GRCh37.p13 chr5: 171,160,105-171,256,604 LOC105377724, LOC105377725, 2 more genes
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6297460copy number variation1nstd186human GRCh37 chr5: 171,219,995-171,220,645 , GRCh38.p12 chr5: 171,792,991-171,793,641 LOC105377725
    nsv6136090copy number variation1nstd213human GRCh37 chr5: 161,030,000-172,600,001 , GRCh38.p12 chr5: 161,602,994-173,172,998 BNIP1, CCNG1, 130 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5897033copy number variation1nstd209human GRCh38 chr5: 171,800,711-171,801,394 , GRCh37.p13 chr5: 171,227,715-171,228,398 LOC105377725
    nsv5464918copy number variation1nstd206human GRCh38 chr5: 171,808,508-171,808,574 , GRCh37.p13 chr5: 171,235,512-171,235,578 LOC105377725
    nsv5462611copy number variation1nstd206human GRCh38 chr5: 171,792,991-171,793,641 , GRCh37.p13 chr5: 171,219,995-171,220,645 LOC105377725
    nsv5454050copy number variation1nstd206human GRCh38 chr5: 171,808,616-171,809,157 , GRCh37.p13 chr5: 171,235,620-171,236,161 LOC105377725
    nsv5362697translocation1nstd200human GRCh38 chr5: 171,793,641-171,793,641 , GRCh38 chr5: 171,792,989-171,792,989 , GRCh37.p13 chr5: 171,219,993-171,219,993 , GRCh37.p13 chr5: 171,220,645-171,220,645 LOC105377725
    nsv5306992copy number variation1nstd204human GRCh38.p13 chr5: 171,833,145-171,835,165 , GRCh37.p13 chr5: 171,260,149-171,262,169 LOC105377725
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