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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
    nsv7076310inversion1nstd229human GRCh38 chr18: 7,168,687-9,983,107 , GRCh37.p13 chr18: 7,168,686-9,983,104 MTCL1, LOC112577592, 40 more genes
    nsv7075855inversion1nstd229human GRCh38 chr18: 6,609,506-9,295,232 , GRCh37.p13 chr18: 6,609,505-9,295,230 LAMA1, RAB12, 28 more genes
    nsv7074186inversion1nstd229human GRCh38 chr18: 7,953,048-15,343,982 , GRCh37.p13 chr18: 7,953,046-15,343,981 PSMG2, EIF4A2P1, 155 more genes
    nsv7065817inversion1nstd229human GRCh38 chr18: 6,839,495-9,543,414 , GRCh37.p13 chr18: 6,839,494-9,543,412 ANKRD12, RPS4XP19, 32 more genes
    nsv7064359inversion1nstd229human GRCh38 chr18: 8,362,600-8,362,617 , GRCh37.p13 chr18: 8,362,598-8,362,615 LOC100192426, PTPRM
    nsv7063411inversion1nstd229human GRCh38 chr18: 7,065,613-8,554,097 , GRCh37.p13 chr18: 7,065,612-8,554,095 AKR1B1P6, LOC112577592, 13 more genes
    nsv7017775copy number variation1nstd229human GRCh38 chr18: 8,077,473-8,592,218 , GRCh37.p13 chr18: 8,077,471-8,592,216 THEMIS3P, LOC100192426, 5 more genes
    nsv7016630copy number variation1nstd229human GRCh38 chr18: 7,408,401-8,729,000 , GRCh37.p13 chr18: 7,408,399-8,728,998 COP1P1, LOC100192426, 11 more genes
    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
    nsv7013857copy number variation1nstd229human GRCh38 chr18: 8,268,714-8,422,616 , GRCh37.p13 chr18: 8,268,712-8,422,614 COP1P1, LOC100192426, 1 more genes
    nsv7013260copy number variation1nstd229human GRCh38 chr18: 8,353,001-8,359,800 , GRCh37.p13 chr18: 8,352,999-8,359,798 LOC100192426, PTPRM
    nsv7003806copy number variation1nstd229human GRCh38 chr18: 8,232,508-8,494,482 , GRCh37.p13 chr18: 8,232,506-8,494,480 COP1P1, RN7SL50P, 2 more genes
    nsv6637924copy number variation1nstd102humanUncertain significance GRCh37 chr18: 8,297,072-8,506,704 , GRCh38.p12 chr18: 8,297,074-8,506,706 RN7SL50P, COP1P1, 2 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
    nsv6624827copy number variation1nstd224human GRCh37 chr18: 8,131,181-8,564,139 , GRCh38.p12 chr18: 8,131,183-8,564,141 PTPRM, COP1P1, 5 more genes
    nsv6624670copy number variation1nstd224human GRCh37 chr18: 8,298,633-8,501,545 , GRCh38.p12 chr18: 8,298,635-8,501,547 PTPRM, LOC100192426, 2 more genes
    nsv6518902copy number variation1nstd223human GRCh38 chr18: 8,268,701-8,422,500 , GRCh37.p13 chr18: 8,268,699-8,422,498 PTPRM, COP1P1, 1 more genes
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