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Items: 1 to 20 of 135

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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
    nsv7043766inversion1nstd229human GRCh38 chr5: 158,447,259-160,356,138 , GRCh37.p13 chr5: 157,874,267-159,783,145 ADRA1B, LOC105377687, 27 more genes
    nsv6797088copy number variation1nstd229human GRCh38 chr5: 160,341,501-160,346,100 , GRCh37.p13 chr5: 159,768,508-159,773,107 C1QTNF2
    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
    nsv6787723copy number variation1nstd229human GRCh38 chr5: 160,361,588-160,365,355 , GRCh37.p13 chr5: 159,788,595-159,792,362 C1QTNF2
    nsv6787298copy number variation1nstd229human GRCh38 chr5: 160,349,066-160,349,435 , GRCh37.p13 chr5: 159,776,073-159,776,442 C1QTNF2
    nsv6782109copy number variation1nstd229human GRCh38 chr5: 160,360,403-160,360,501 , GRCh37.p13 chr5: 159,787,410-159,787,508 C1QTNF2
    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
    nsv6570436inversion1nstd223human GRCh38 chr5: 160,353,907-160,354,510 , GRCh37.p13 chr5: 159,780,914-159,781,517 C1QTNF2
    nsv6405717copy number variation1nstd223human GRCh38 chr5: 160,341,539-160,346,107 , GRCh37.p13 chr5: 159,768,546-159,773,114 C1QTNF2
    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
    nsv6315317copy number variation1nstd102humanUncertain significance GRCh38 chr5: 158,887,731-164,722,046 , GRCh37.p13 chr5: 158,314,739-164,149,052 LINC03000, SNRPEP1, 64 more genes
    nsv6290966copy number variation1nstd102humannot provided GRCh37 chr5: 155,970,607-162,450,579 , GRCh38.p12 chr5: 156,543,597-163,023,573 C1QTNF2, MED7, 86 more genes
    nsv6135662copy number variation1nstd213human GRCh37 chr5: 159,690,000-159,790,001 , GRCh38.p12 chr5: 160,262,993-160,362,994 CCNJL, C1QTNF2, 2 more genes
    nsv6135660copy number variation1nstd213human GRCh37 chr5: 158,750,000-159,990,001 , GRCh38.p12 chr5: 159,322,992-160,562,994 ADRA1B, FABP6, 25 more genes
    nsv6135632copy number variation1nstd213human GRCh37 chr5: 159,693,227-159,772,829 , GRCh38.p12 chr5: 160,266,220-160,345,822 CCNJL, C1QTNF2, 2 more genes
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