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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077246inversion1nstd229human GRCh38 chr15: 64,487,767-67,498,498 , GRCh37.p13 chr15: 64,779,966-67,790,836 LETM1P1, MIR4512, 74 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7069168inversion1nstd229human GRCh38 chr15: 65,085,774-67,006,275 , GRCh37.p13 chr15: 65,378,112-67,298,613 MEGF11, HNRNPA1P44, 51 more genes
    nsv6967827copy number variation1nstd229human GRCh38 chr15: 66,386,041-66,735,404 , GRCh37.p13 chr15: 66,678,379-67,027,742 ATP5MFP6, SMAD6, 13 more genes
    nsv6309802copy number variation2nstd102humanUncertain significance GRCh37 chr15: 66,161,924-69,018,313 , GRCh38.p12 chr15: 65,869,586-68,725,974 SNORD18B, TRQ-CTG1-4, 50 more genes
    nsv6309736copy number variation1nstd102humanUncertain significance GRCh37 chr15: 66,774,083-66,782,963 , GRCh38.p12 chr15: 66,481,745-66,490,625 SNAPC5, MAP2K1
    nsv6133153copy number variation1nstd213human GRCh37 chr15: 66,740,000-66,910,001 , GRCh38.p12 chr15: 66,447,662-66,617,663 MAP2K1, RPL4, 9 more genes
    nsv6095344insertion1nstd212human GRCh38 chr15: 66,491,246-66,491,246 , GRCh37.p13 chr15: 66,783,584-66,783,584 MAP2K1, SNAPC5
    nsv5380765copy number variation1nstd102humanUncertain significance GRCh37 chr15: 66,679,676-66,782,963 , GRCh38.p12 chr15: 66,387,338-66,490,625 MAP2K1, TIPIN, 3 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5380136translocation1nstd200human GRCh38 chr15: 66,497,914-66,497,914 , GRCh38 chr15: 66,497,504-66,497,504 , GRCh37.p13 chr15: 66,790,252-66,790,252 , GRCh37.p13 chr15: 66,789,842-66,789,842 RPL4, SNAPC5, 1 more genes
    nsv5380135translocation1nstd200human GRCh38 chr15: 66,497,914-66,497,914 , GRCh38 chr15: 66,492,847-66,492,847 , GRCh37.p13 chr15: 66,790,252-66,790,252 , GRCh37.p13 chr15: 66,785,185-66,785,185 RPL4, SNAPC5
    nsv5340148translocation1nstd200human GRCh37 chr15: 66,790,252-66,790,252 , GRCh37 chr15: 66,785,185-66,785,185 , GRCh38.p12 chr15: 66,492,847-66,492,847 , GRCh38.p12 chr15: 66,497,914-66,497,914 SNAPC5, RPL4
    nsv5339936translocation1nstd200human GRCh37 chr15: 66,789,842-66,789,842 , GRCh37 chr15: 66,790,252-66,790,252 , GRCh38.p12 chr15: 66,497,914-66,497,914 , GRCh38.p12 chr15: 66,497,504-66,497,504 RPL4, SNAPC5, 1 more genes
    nsv5142244mobile element insertion1nstd203human GRCh38 chr15: 66,490,747-66,490,764 , GRCh37.p13 chr15: 66,783,085-66,783,102 SNAPC5, MAP2K1
    nsv4992088copy number variation1nstd200human GRCh38 chr15: 66,488,096-66,488,175 , GRCh37.p13 chr15: 66,780,434-66,780,513 MAP2K1, SNAPC5
    nsv4375713copy number variation1nstd173human GRCh37 chr15: 66,354,432-66,790,939 , GRCh38.p12 chr15: 66,062,094-66,498,601 , GRCh38.p12 chr15|NW_003315944.2: 153,912-388,773 SNAPC5, TIPIN, 10 more genes
    nsv4375434copy number variation1nstd173human GRCh37 chr15: 66,356,282-66,790,939 , GRCh38.p12 chr15: 66,063,944-66,498,601 , GRCh38.p12 chr15|NW_003315944.2: 155,762-388,773 RPL4, MIR4512, 10 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
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