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Items: 1 to 20 of 279

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093376copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 156,786,013-162,945,369 , GRCh38.p12 chr5: 157,359,005-163,518,363 ADRA1B, CCNG1, 81 more genes
    nsv7057344inversion1nstd229human GRCh38 chr5: 158,420,376-160,356,139 , GRCh37.p13 chr5: 157,847,384-159,783,146 LINC01845, TTC1, 27 more genes
    nsv7054438inversion1nstd229human GRCh38 chr5: 158,806,124-160,433,845 , GRCh37.p13 chr5: 158,233,132-159,860,852 LINC01845, TTC1, 30 more genes
    nsv7050992inversion1nstd229human GRCh38 chr5: 160,189,896-160,211,462 , GRCh37.p13 chr5: 159,616,903-159,638,469 FABP6-AS1, FABP6
    nsv7043766inversion1nstd229human GRCh38 chr5: 158,447,259-160,356,138 , GRCh37.p13 chr5: 157,874,267-159,783,145 ADRA1B, LOC105377687, 27 more genes
    nsv6794984copy number variation1nstd229human GRCh38 chr5: 159,275,371-163,261,193 , GRCh37.p13 chr5: 158,702,379-162,688,199 LOC105377685, CCNJL, 45 more genes
    nsv6794502copy number variation1nstd229human GRCh38 chr5: 160,216,258-160,219,565 , GRCh37.p13 chr5: 159,643,265-159,646,572 FABP6
    nsv6790437copy number variation1nstd229human GRCh38 chr5: 160,137,201-160,213,000 , GRCh37.p13 chr5: 159,564,208-159,640,007 FABP6, FABP6-AS1
    nsv6787904copy number variation1nstd229human GRCh38 chr5: 160,182,701-160,190,400 , GRCh37.p13 chr5: 159,609,708-159,617,407 FABP6
    nsv6787825copy number variation1nstd229human GRCh38 chr5: 160,218,493-160,221,403 , GRCh37.p13 chr5: 159,645,500-159,648,410 FABP6
    nsv6787073copy number variation1nstd229human GRCh38 chr5: 160,220,907-160,226,381 , GRCh37.p13 chr5: 159,647,914-159,653,388 FABP6
    nsv6781237copy number variation1nstd229human GRCh38 chr5: 160,080,001-160,394,000 , GRCh37.p13 chr5: 159,507,008-159,821,007 FABP6-AS1, C1QTNF2, 7 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
    nsv6636858copy number variation1nstd102humanUncertain significance GRCh37 chr5: 159,535,230-161,656,766 , GRCh38.p12 chr5: 160,108,223-162,229,760 MIR146A, SNRPEP1, 23 more genes
    nsv6414394copy number variation1nstd223human GRCh38 chr5: 160,226,401-160,227,600 , GRCh37.p13 chr5: 159,653,408-159,654,607 FABP6
    nsv6414196copy number variation1nstd223human GRCh38 chr5: 160,182,745-160,189,342 , GRCh37.p13 chr5: 159,609,752-159,616,349 FABP6
    nsv6407980copy number variation1nstd223human GRCh38 chr5: 160,195,899-160,197,054 , GRCh37.p13 chr5: 159,622,906-159,624,061 FABP6-AS1, FABP6
    nsv6401338copy number variation1nstd223human GRCh38 chr5: 160,199,120-160,265,803 , GRCh37.p13 chr5: 159,626,127-159,692,810 LOC105377691, CCNJL, 3 more genes
    nsv6399161copy number variation1nstd223human GRCh38 chr5: 160,199,201-160,199,800 , GRCh37.p13 chr5: 159,626,208-159,626,807 FABP6, FABP6-AS1
    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
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