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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117396mobile element insertion1nstd186human GRCh37 chr14: 48,230,226-48,230,263 , GRCh38.p12 chr14: 47,761,023-47,761,060 MIR548Y
    nsv5940619copy number variation1nstd209human GRCh38 chr14: 41,756,659-48,371,099 , GRCh37.p13 chr14: 42,225,862-48,840,302 LOC100418768, RNU6-297P, 53 more genes
    nsv5938242copy number variation1nstd209human GRCh38 chr14: 47,760,609-47,808,195 , GRCh37.p13 chr14: 48,229,812-48,277,398 LOC100420098, MIR548Y, 1 more genes
    nsv5935089copy number variation1nstd209human GRCh38 chr14: 46,941,699-52,127,962 , GRCh37.p13 chr14: 47,410,902-52,594,680 , RNA5SP385, 92 more genes
    nsv5866425copy number variation1nstd209human GRCh38 chr14: 47,760,899-47,775,289 , GRCh37.p13 chr14: 48,230,102-48,244,492 MIR548Y, LINC00648
    nsv5696502mobile element insertion1nstd211human GRCh38 chr14: 47,761,025-47,761,025 , GRCh37.p13 chr14: 48,230,228-48,230,228 MIR548Y
    nsv5505386copy number variation1nstd206human GRCh38 chr14: 47,760,613-47,808,196 , GRCh37.p13 chr14: 48,229,816-48,277,399 LOC100420098, LINC00648, 1 more genes
    nsv5426605mobile element insertion1nstd206human GRCh38 chr14: 47,761,023-47,761,060 , GRCh37.p13 chr14: 48,230,226-48,230,263 MIR548Y
    nsv5317868copy number variation1nstd204human GRCh37.p13 chr14: 48,229,806-48,277,403 , GRCh38.p13 chr14: 47,760,603-47,808,200 LOC100420098, MIR548Y, 1 more genes
    nsv5270504copy number variation1nstd204human GRCh38.p13 chr14: 47,760,601-47,808,200 , GRCh37.p13 chr14: 48,229,804-48,277,403 LINC00648, MIR548Y, 1 more genes
    nsv5267476copy number variation1nstd204human GRCh38.p13 chr14: 47,761,299-47,807,018 , GRCh37.p13 chr14: 48,230,502-48,276,221 LINC00648, LOC100420098, 1 more genes
    nsv4999230copy number variation1nstd200human GRCh38 chr14: 47,760,613-47,808,196 , GRCh37.p13 chr14: 48,229,816-48,277,399 MIR548Y, LOC100420098, 1 more genes
    nsv4833611copy number variation1nstd200human GRCh37 chr14: 48,229,816-48,277,399 , GRCh38.p12 chr14: 47,760,613-47,808,196 MIR548Y, LOC100420098, 1 more genes
    nsv4622494copy number variation1nstd183human GRCh37 chr14: 48,227,037-48,277,451 , GRCh38.p12 chr14: 47,757,834-47,808,248 LINC00648, LOC100420098, 1 more genes
    nsv4621755copy number variation1nstd183human GRCh37 chr14: 48,229,812-48,277,399 , GRCh38.p12 chr14: 47,760,609-47,808,196 MIR548Y, LINC00648, 1 more genes
    nsv4456026copy number variation1nstd102humanUncertain significance GRCh37 chr14: 48,120,308-48,277,276 , GRCh38.p12 chr14: 47,651,105-47,808,073 MDGA2, LOC100420098, 2 more genes
    nsv4422765copy number variation1nstd174human GRCh37 chr14: 48,224,031-48,286,588 , GRCh38.p12 chr14: 47,754,828-47,817,385 LINC00648, MIR548Y, 1 more genes
    nsv4384720copy number variation1nstd173human GRCh37 chr14: 48,227,126-48,277,484 , GRCh38.p12 chr14: 47,757,923-47,808,281 LOC100420098, MIR548Y, 1 more genes
    nsv4371458copy number variation5nstd173human GRCh37 chr14: 48,227,114-48,277,484 , GRCh38.p12 chr14: 47,757,911-47,808,281 MIR548Y, LOC100420098, 1 more genes
    nsv4368491copy number variation6nstd173human GRCh37 chr14: 48,227,024-48,277,484 , GRCh38.p12 chr14: 47,757,821-47,808,281 LOC100420098, MIR548Y, 1 more genes
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