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Items: 1 to 20 of 262

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148271copy number variation1nstd102humanPathogenic GRCh38 chr18: 158,286-14,124,574 , GRCh37.p13 chr18: 158,286-14,124,573 PMM2P2, EIF4A2P1, 225 more genes
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv7077004inversion1nstd229human GRCh38 chr18: 5,041,429-5,620,611 , GRCh37.p13 chr18: 5,041,428-5,620,610 ZBTB14, BOD1P2, 10 more genes
    nsv7072282inversion1nstd229human GRCh38 chr18: 5,225,526-5,700,194 , GRCh37.p13 chr18: 5,225,525-5,700,193 LOC100422274, LOC107985144, 7 more genes
    nsv7017026copy number variation1nstd229human GRCh38 chr18: 5,237,201-5,238,900 , GRCh37.p13 chr18: 5,237,200-5,238,899 LINC00667, LOC100422274, 1 more genes
    nsv7016177copy number variation1nstd229human GRCh38 chr18: 5,238,501-5,242,100 , GRCh37.p13 chr18: 5,238,500-5,242,099 LINC00667, LOC100422274, 1 more genes
    nsv7015370copy number variation1nstd229human GRCh38 chr18: 5,224,601-5,238,100 , GRCh37.p13 chr18: 5,224,600-5,238,099 LINC00667, LINC00526
    nsv7015128copy number variation1nstd229human GRCh38 chr18: 4,434,377-14,413,632 , GRCh37.p13 chr18: 4,434,377-14,413,631 RAB31, THEMIS3P, 167 more genes
    nsv6638021copy number variation1nstd102humanUncertain significance GRCh37 chr18: 3,824,312-6,983,454 , GRCh38.p12 chr18: 3,824,312-6,983,455 MIR3976, GAPDHP66, 40 more genes
    nsv6637580copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-7,218,594 , GRCh38.p12 chr18: 136,227-7,218,596 L3MBTL4-AS1, LOC101927044, 106 more genes
    nsv6637285copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-11,283,184 , GRCh38.p12 chr18: 136,227-11,283,185 EMILIN2, KRT18P8, 165 more genes
    nsv6634418copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-8,638,260 , GRCh38.p12 chr18: 10,001-8,638,262 AKAIN1, LPIN2, 126 more genes
    nsv6585584inversion1nstd223human GRCh38 chr18: 3,134,944-5,291,746 , GRCh37.p13 chr18: 3,134,942-5,291,745 LINC00667, LINC01895, 33 more genes
    nsv6315536copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-10,172,941 , GRCh38.p12 chr18: 136,226-10,172,944 DLGAP1-AS5, TWSG1, 150 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6315508copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-14,632,436 , GRCh38.p12 chr18: 136,226-14,632,437 IGLJCOR18, MYOM1, 247 more genes
    nsv6315472copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-7,131,132 , GRCh38.p12 chr18: 136,226-7,131,133 LOC105371963, YES1, 105 more genes
    nsv6315187copy number variation1nstd102humanPathogenic GRCh37 chr18: 47,390-14,854,037 , GRCh38.p12 chr18: 47,390-14,854,038 MIR4526, LINC01882, 261 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6314165copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-6,103,499 , GRCh38.p12 chr18: 136,226-6,103,500 SMCHD1, LOC105371953, 90 more genes
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