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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048370inversion1nstd229human GRCh38 chr5: 31,943,969-32,642,096 , GRCh37.p13 chr5: 31,944,075-32,642,202 RPL27P10, GOLPH3, 10 more genes
    nsv7048024inversion1nstd229human GRCh38 chr5: 32,209,920-32,225,737 , GRCh37.p13 chr5: 32,210,026-32,225,843 RPL27P10, MTMR12
    nsv7040255inversion1nstd229human GRCh38 chr5: 32,230,717-32,230,842 , GRCh37.p13 chr5: 32,230,823-32,230,948 MTMR12
    nsv7038918inversion1nstd229human GRCh38 chr5: 31,932,933-32,628,546 , GRCh37.p13 chr5: 31,933,039-32,628,652 RNU6-378P, RPL27P10, 10 more genes
    nsv6773413copy number variation1nstd229human GRCh38 chr5: 32,281,254-32,283,399 , GRCh37.p13 chr5: 32,281,360-32,283,505 MTMR12
    nsv6770193copy number variation1nstd229human GRCh38 chr5: 32,302,738-32,302,778 , GRCh37.p13 chr5: 32,302,844-32,302,884 MTMR12
    nsv6770174copy number variation1nstd229human GRCh38 chr5: 32,170,252-32,417,269 , GRCh37.p13 chr5: 32,170,358-32,417,374 GOLPH3, RNU6-1079P, 5 more genes
    nsv6766726copy number variation1nstd229human GRCh38 chr5: 32,302,280-32,306,650 , GRCh37.p13 chr5: 32,302,386-32,306,756 MTMR12
    nsv6765548copy number variation1nstd229human GRCh38 chr5: 32,290,310-32,298,245 , GRCh37.p13 chr5: 32,290,416-32,298,351 MTMR12
    nsv6762717copy number variation1nstd229human GRCh38 chr5: 32,195,713-32,417,756 , GRCh37.p13 chr5: 32,195,819-32,417,861 MTMR12, MIR579, 4 more genes
    nsv6760000copy number variation1nstd229human GRCh38 chr5: 32,260,034-32,261,144 , GRCh37.p13 chr5: 32,260,140-32,261,250 MTMR12
    nsv6759367copy number variation1nstd229human GRCh38 chr5: 32,267,128-32,268,259 , GRCh37.p13 chr5: 32,267,234-32,268,365 MTMR12
    nsv6759333copy number variation1nstd229human GRCh38 chr5: 32,248,708-32,248,790 , GRCh37.p13 chr5: 32,248,814-32,248,896 MTMR12
    nsv6758447copy number variation1nstd229human GRCh38 chr5: 32,310,052-32,312,036 , GRCh37.p13 chr5: 32,310,158-32,312,142 MTMR12, RNU6-378P
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6573332inversion1nstd223human GRCh38 chr5: 32,266,938-32,269,272 , GRCh37.p13 chr5: 32,267,044-32,269,378 MTMR12
    nsv6568133inversion1nstd223human GRCh38 chr5: 32,267,189-32,269,208 , GRCh37.p13 chr5: 32,267,295-32,269,314 MTMR12
    nsv6563745inversion1nstd223human GRCh38 chr5: 32,308,336-32,308,886 , GRCh37.p13 chr5: 32,308,442-32,308,992 RNU6-378P, MTMR12
    nsv6563394inversion1nstd223human GRCh38 chr5: 32,268,374-32,269,154 , GRCh37.p13 chr5: 32,268,480-32,269,260 MTMR12
    nsv6563348inversion1nstd223human GRCh38 chr5: 32,267,355-32,268,023 , GRCh37.p13 chr5: 32,267,461-32,268,129 MTMR12
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