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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075997inversion1nstd229human GRCh38 chr8: 56,110,814-56,120,688 , GRCh37.p13 chr8: 57,023,373-57,033,247 MOS
    nsv7072857inversion1nstd229human GRCh38 chr8: 56,111,369-56,115,945 , GRCh37.p13 chr8: 57,023,928-57,028,504 MOS
    nsv7067508inversion1nstd229human GRCh38 chr8: 51,755,366-56,976,322 , GRCh37.p13 chr8: 52,667,926-57,888,881 CHCHD2P10, LOC105375850, 81 more genes
    nsv7064051inversion1nstd229human GRCh38 chr8: 53,370,406-56,357,942 , GRCh37.p13 chr8: 54,282,966-57,270,501 CHCHD2P10, RN7SL798P, 51 more genes
    nsv6854491copy number variation1nstd229human GRCh38 chr8: 56,012,001-56,140,200 , GRCh37.p13 chr8: 56,924,560-57,052,759 MOS, PSMC6P1, 6 more genes
    nsv6569954inversion1nstd223human GRCh38 chr8: 50,962,824-58,188,676 , GRCh37.p13 chr8: 51,875,384-59,101,235 LOC101929398, LOC107986888, 98 more genes
    nsv6312728copy number variation1nstd102humanUncertain significance GRCh37 chr8: 56,854,419-57,906,144 , GRCh38.p12 chr8: 55,941,860-56,993,585 CERNA3, RN7SL798P, 24 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136065copy number variation1nstd213human GRCh37 chr8: 56,820,000-59,400,001 , GRCh38.p12 chr8: 55,907,441-58,487,442 LYN, MOS, 42 more genes
    nsv6136061copy number variation1nstd213human GRCh37 chr8: 54,780,000-63,060,001 , GRCh38.p12 chr8: 53,867,440-62,147,442 RAB2A, SDCBP, 117 more genes
    nsv4680675copy number variation1nstd189human GRCh37.p13 chr8: 56,753,727-57,051,296 , GRCh38.p12 chr8: 55,841,168-56,138,737 LYN, MOS, 8 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
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4345425sequence alteration1nstd166human GRCh37.p13 chr8: 57,023,372-57,033,246 , GRCh38.p12 chr8: 56,110,813-56,120,687 MOS
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv3924755copy number variation1nstd102humanPathogenic NCBI36 chr8: 50,546,890-58,900,583 , GRCh37 chr8: 50,384,337-58,738,029 , GRCh38 chr8: 49,471,778-57,825,470 LOC105375849, RP1, 103 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
    nsv3923501copy number variation1nstd102humanPathogenic NCBI36 chr8: 55,896,471-62,221,415 , GRCh38 chr8: 54,821,357-61,146,302 , GRCh37 chr8: 55,733,917-62,058,861 NUDT15P1, LINC01301, 83 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
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