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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5926037copy number variation1nstd209human GRCh38 chr8: 42,390,280-42,390,384 , GRCh37.p13 chr8: 42,247,798-42,247,902 DKK4, VDAC3
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5492900copy number variation1nstd206human GRCh38 chr8: 42,390,280-42,390,385 , GRCh37.p13 chr8: 42,247,798-42,247,903 DKK4, VDAC3
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4967160copy number variation1nstd200human GRCh38 chr8: 42,391,528-42,391,609 , GRCh37.p13 chr8: 42,249,046-42,249,127 VDAC3, DKK4
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4715870copy number variation1nstd195human GRCh38.p12 chr8: 42,296,283-42,684,308 , GRCh37 chr8: 42,153,801-42,539,451 IKBKB, POLB, 6 more genes
    nsv4674828copy number variation1nstd102humanUncertain significance GRCh37 chr8: 42,143,121-42,353,003 , GRCh38.p12 chr8: 42,285,603-42,495,485 RPL5P23, POLB, 5 more genes
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456199copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,094,421-43,822,214 , GRCh38.p12 chr8: 36,236,903-43,967,071 AFG3L2P1, BRF2, 136 more genes
    nsv4451189copy number variation1nstd102humanUncertain significance GRCh37 chr8: 42,128,869-43,054,732 , GRCh38.p12 chr8: 42,271,351-43,199,589 RPL5P23, RNF170, 21 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4171410copy number variation1nstd166human GRCh37.p13 chr8: 42,247,798-42,247,887 , GRCh38.p12 chr8: 42,390,280-42,390,369 VDAC3, DKK4
    nsv3924648copy number variation1nstd102humanPathogenic NCBI36 chr8: 39,937,207-43,647,507 , GRCh37 chr8: 39,818,050-43,528,350 , GRCh38 chr8: 39,960,531-43,673,207 IDO2, NKX6-3, 68 more genes
    nsv3923517copy number variation1nstd102humanPathogenic NCBI36 chr8: 36,556,779-60,694,111 , GRCh37 chr8: 36,437,621-60,531,557 , GRCh38 chr8: 36,580,103-59,618,998 LOC105379380, TPT1P8, 320 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3922311copy number variation1nstd102humanPathogenic NCBI36 chr8: 37,428,611-47,058,107 , GRCh37.p13 chr8: 37,309,453-46,938,942 , GRCh38.p12 chr8: 37,451,935-46,027,320 CHRNB3, LOC105379380, 120 more genes
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