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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672807copy number variation1nstd102humanPathogenic GRCh37 chr13: 92,002,837-103,343,314 , GRCh38.p12 chr13: 91,350,583-102,690,964 RPL7L1P12, MIR548AS, 153 more genes
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5504483copy number variation1nstd206human GRCh38 chr13: 99,984,564-99,984,784 , GRCh37.p13 chr13: 100,636,818-100,637,038 ZIC2
    nsv5310238copy number variation1nstd204human GRCh38.p13 chr13: 99,780,247-99,980,185 , GRCh37.p13 chr13: 100,432,501-100,632,439 CLYBL, CLYBL-AS3, 2 more genes
    nsv5268134copy number variation1nstd204human GRCh38.p13 chr13: 99,780,101-99,980,200 , GRCh37.p13 chr13: 100,432,355-100,632,454 ZIC2, ZIC5, 2 more genes
    nsv5264128copy number variation1nstd204human GRCh38.p13 chr13: 99,983,285-99,987,416 , GRCh37.p13 chr13: 100,635,539-100,639,670 ZIC2
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4845296copy number variation1nstd200human GRCh37 chr13: 100,432,504-100,632,430 , GRCh38.p12 chr13: 99,780,250-99,980,176 CLYBL-AS3, ZIC2, 2 more genes
    nsv4683528copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,038,233-100,638,902 , GRCh38.p12 chr13: 99,385,979-99,986,648 CLYBL-AS2, RNY3P6, 14 more genes
    nsv4675892copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,240,346-106,103,782 , GRCh38.p12 chr13: 95,588,092-105,451,433 LOC105370328, LINC00554, 132 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4675644copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258 ZIC2, LINC03032, 266 more genes
    nsv4599052copy number variation1nstd183human GRCh37 chr13: 100,637,889-100,638,358 , GRCh38.p12 chr13: 99,985,635-99,986,104 ZIC2
    nsv4456561copy number variation1nstd102humanPathogenic GRCh37 chr13: 61,775,567-115,107,733 , GRCh38.p12 chr13: 61,201,433-114,342,258 LOC105370262, LINC01080, 609 more genes
    nsv4456260copy number variation1nstd102humanUncertain significance GRCh37 chr13: 94,849,303-115,107,733 , GRCh38.p12 chr13: 94,197,049-114,342,258 F10, FKSG29, 300 more genes
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 LOC105370271, OR7E33P, 925 more genes
    nsv3923796copy number variation1nstd102humanPathogenic NCBI36 chr13: 78,471,454-114,110,683 , GRCh38 chr13: 78,999,318-114,327,106 , GRCh37 chr13: 79,573,453-115,085,141 LOC107984608, TEX29, 423 more genes
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