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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148269copy number variation1nstd102humanPathogenic GRCh38 chr8: 37,814,644-38,528,889 , GRCh37.p13 chr8: 37,672,162-38,386,407 GOT1L1, FGFR1, 20 more genes
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7060611inversion1nstd229human GRCh38 chr8: 38,008,386-38,052,499 , GRCh37.p13 chr8: 37,865,904-37,910,017 EIF4EBP1
    nsv6852516copy number variation1nstd229human GRCh38 chr8: 38,034,276-38,036,879 , GRCh37.p13 chr8: 37,891,794-37,894,397 EIF4EBP1
    nsv6849109copy number variation1nstd229human GRCh38 chr8: 38,049,771-38,051,833 , GRCh37.p13 chr8: 37,907,289-37,909,351 EIF4EBP1
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6575572inversion1nstd223human GRCh38 chr8: 38,059,774-38,060,745 , GRCh37.p13 chr8: 37,917,292-37,918,263 EIF4EBP1
    nsv6575512inversion1nstd223human GRCh38 chr8: 37,994,343-38,032,464 , GRCh37.p13 chr8: 37,851,861-37,889,982 EIF4EBP1
    nsv6568261inversion1nstd223human GRCh38 chr8: 38,032,227-38,033,216 , GRCh37.p13 chr8: 37,889,745-37,890,734 EIF4EBP1
    nsv6561606inversion1nstd223human GRCh38 chr8: 38,059,016-38,060,740 , GRCh37.p13 chr8: 37,916,534-37,918,258 EIF4EBP1
    nsv6556578inversion1nstd223human GRCh38 chr8: 38,059,820-38,059,973 , GRCh37.p13 chr8: 37,917,338-37,917,491 EIF4EBP1
    nsv6432756copy number variation1nstd223human GRCh38 chr8: 38,043,568-38,046,067 , GRCh37.p13 chr8: 37,901,086-37,903,585 EIF4EBP1
    nsv6422995copy number variation1nstd223human GRCh38 chr8: 38,035,321-38,035,813 , GRCh37.p13 chr8: 37,892,839-37,893,331 EIF4EBP1
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6312909copy number variation5nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 37,595,441-38,961,219 , GRCh38.p12 chr8: 37,737,923-39,103,700 LSM1, BAG4, 33 more genes
    nsv6137281copy number variation1nstd213human GRCh37 chr8: 37,350,000-38,410,001 , GRCh38.p12 chr8: 37,492,482-38,552,483 ADRB3, EIF4EBP1, 32 more genes
    nsv6136673copy number variation1nstd213human GRCh37 chr8: 37,880,000-38,230,001 , GRCh38.p12 chr8: 38,022,482-38,372,483 STAR, ASH2L, 9 more genes
    nsv6002937copy number variation1nstd212human GRCh38 chr8: 38,038,372-38,038,449 , GRCh37.p13 chr8: 37,895,890-37,895,967 EIF4EBP1
    nsv5950587insertion1nstd209human GRCh38 chr8: 38,052,417-38,052,417 , GRCh37.p13 chr8: 37,909,935-37,909,935 EIF4EBP1
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