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Items: 1 to 20 of 946

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095443copy number variation1nstd102humanUncertain significance GRCh37 chr18: 32,335,941-32,464,709 , GRCh38.p12 chr18: 34,755,977-34,884,745 DTNA
    nsv7074645inversion1nstd229human GRCh38 chr18: 30,537,670-35,063,371 , GRCh37.p13 chr18: 28,117,636-32,643,335 DSC1, RN7SKP44, 46 more genes
    nsv7069076inversion1nstd229human GRCh38 chr18: 34,706,436-34,706,538 , GRCh37.p13 chr18: 32,286,400-32,286,502 DTNA
    nsv7062971inversion1nstd229human GRCh38 chr18: 34,731,698-34,736,399 , GRCh37.p13 chr18: 32,311,662-32,316,363 DTNA
    nsv7060254inversion1nstd229human GRCh38 chr18: 34,732,670-34,733,996 , GRCh37.p13 chr18: 32,312,634-32,313,960 DTNA
    nsv7016963copy number variation1nstd229human GRCh38 chr18: 34,515,401-34,518,400 , GRCh37.p13 chr18: 32,095,365-32,098,364 DTNA
    nsv7013090copy number variation1nstd229human GRCh38 chr18: 34,527,560-34,533,580 , GRCh37.p13 chr18: 32,107,524-32,113,544 DTNA
    nsv7012844copy number variation1nstd229human GRCh38 chr18: 34,564,159-34,573,908 , GRCh37.p13 chr18: 32,144,123-32,153,872 DTNA, RPL10AP13
    nsv7012821copy number variation1nstd229human GRCh38 chr18: 34,613,447-34,617,496 , GRCh37.p13 chr18: 32,193,411-32,197,460 DTNA
    nsv7011318copy number variation1nstd229human GRCh38 chr18: 34,582,051-34,588,081 , GRCh37.p13 chr18: 32,162,015-32,168,045 DTNA
    nsv7010674copy number variation1nstd229human GRCh38 chr18: 34,807,872-34,811,024 , GRCh37.p13 chr18: 32,387,836-32,390,988 DTNA
    nsv7009638copy number variation1nstd229human GRCh38 chr18: 34,846,176-34,846,955 , GRCh37.p13 chr18: 32,426,140-32,426,919 DTNA
    nsv7009296copy number variation1nstd229human GRCh38 chr18: 34,577,543-34,584,258 , GRCh37.p13 chr18: 32,157,507-32,164,222 DTNA
    nsv7009293copy number variation1nstd229human GRCh38 chr18: 34,453,177-37,158,337 , GRCh37.p13 chr18: 32,033,141-34,738,300 LOC105372061, RNU4-3P, 31 more genes
    nsv7007577copy number variation1nstd229human GRCh38 chr18: 34,768,440-34,768,476 , GRCh37.p13 chr18: 32,348,404-32,348,440 DTNA
    nsv7007421copy number variation1nstd229human GRCh38 chr18: 34,674,636-34,674,807 , GRCh37.p13 chr18: 32,254,600-32,254,771 DTNA
    nsv7007387copy number variation1nstd229human GRCh38 chr18: 34,718,310-34,738,162 , GRCh37.p13 chr18: 32,298,274-32,318,126 DTNA
    nsv7007304copy number variation1nstd229human GRCh38 chr18: 34,547,099-34,568,350 , GRCh37.p13 chr18: 32,127,063-32,148,314 DTNA
    nsv7006970copy number variation1nstd229human GRCh38 chr18: 34,705,991-34,717,205 , GRCh37.p13 chr18: 32,285,955-32,297,169 DTNA
    nsv7006914copy number variation1nstd229human GRCh38 chr18: 34,496,984-34,502,458 , GRCh37.p13 chr18: 32,076,948-32,082,422 DTNA
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