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Items: 1 to 20 of 339

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4456944copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,627,916-107,147,698 , GRCh38.p12 chr14: 101,161,579-106,691,681 IGHV3-16, IGHV3-21, 319 more genes
    nsv4456320copy number variation1nstd102humanPathogenic GRCh37 chr14: 102,931,119-107,285,437 , GRCh38.p12 chr14: 102,464,782-106,877,229 MIR12121, CEP170B, 310 more genes
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 RN7SL634P, SNORD114-15, 617 more genes
    nsv4455831copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,067,651-107,285,437 , GRCh38.p12 chr14|NT_187600.1: 1-1,214,078 , GRCh38.p12 chr14: 104,622,881-106,877,229 IGHE, IGHG1, 243 more genes
    nsv4455156copy number variation1nstd102humanPathogenic GRCh37 chr14: 99,794,230-107,285,437 , GRCh38.p12 chr14: 99,327,893-106,877,229 TRAF3, IGHVIII-2-1, 477 more genes
    nsv4436056complex substitution1nstd102humanUncertain significance GRCh38.p12 chr14: 104,177,384-105,466,438 , GRCh37 chr14: 104,643,721-105,932,775 AKT1, BRF1, 36 more genes
    nsv4360423copy number variation1nstd102humanPathogenic NCBI36 chr14: 76,758,891-106,358,550 , GRCh37.p13 chr14: 77,689,138-107,287,505 , GRCh38.p12 chr14: 77,222,795-106,879,298 RPS2P4, IGHJ4, 774 more genes
    nsv4360317copy number variation1nstd102humanUncertain significance NCBI36 chr14: 103,846,616-104,435,928 , GRCh37.p13 chr14: 104,775,571-105,364,883 , GRCh38.p12 chr14: 104,309,234-104,898,546 CEP170B, AKT1, 18 more genes
    nsv4359295copy number variation1nstd102humanPathogenic NCBI36 chr14: 101,201,692-106,334,523 , GRCh37.p13 chr14: 102,131,939-107,263,478 , GRCh38.p12 chr14: 101,665,602-106,855,263 IGHVIII-67-2, IGHV3-20, 324 more genes
    nsv4358774copy number variation1nstd102humanPathogenic NCBI36 chr14: 102,141,186-106,358,550 , GRCh37.p13 chr14: 103,071,433-107,287,505 , GRCh38.p12 chr14: 102,605,096-106,879,298 HOMER2P2, MIR203B, 303 more genes
    nsv4358721copy number variation1nstd102humanPathogenic NCBI36 chr14: 73,192,228-106,358,550 , GRCh37.p13 chr14: 74,122,475-107,287,505 , GRCh38.p12 chr14: 73,655,772-106,879,298 SERPINA13P, IGHV7-27, 874 more genes
    nsv4358695copy number variation1nstd102humanPathogenic NCBI36 chr14: 97,474,727-106,334,523 , GRCh37.p13 chr14: 98,404,974-107,263,478 , GRCh38.p12 chr14: 97,938,637-106,855,263 IGHE, PPP1R13B, 490 more genes
    nsv4358064copy number variation1nstd102humanPathogenic NCBI36 chr14: 102,121,053-104,435,987 , GRCh37.p13 chr14: 103,051,300-105,364,942 , GRCh38.p12 chr14: 102,584,963-104,898,605 MIR203A, SNORA28, 74 more genes
    nsv4357293copy number variation1nstd102humanPathogenic NCBI36 chr14: 100,344,390-106,334,523 , GRCh37.p13 chr14: 101,274,637-107,263,478 , GRCh38.p12 chr14: 100,808,300-106,855,263 IGHD3-10, IGHJ5, 439 more genes
    nsv4357031copy number variation1nstd102humanPathogenic NCBI36 chr14: 102,858,504-106,334,523 , GRCh37.p13 chr14: 103,788,751-107,263,478 , GRCh38.p12 chr14: 103,322,414-106,855,263 ELK2AP, IGHD1-7, 277 more genes
    nsv4356868copy number variation1nstd102humanPathogenic NCBI36 chr14: 95,060,497-106,358,753 , GRCh37.p13 chr14: 95,990,744-107,287,708 , GRCh38.p12 chr14: 95,524,407-106,879,501 IGHV1-3, LOC105370653, 532 more genes
    nsv4355752copy number variation1nstd102humanPathogenic NCBI36 chr14: 19,689,148-106,334,523 , GRCh37.p13 chr14: 20,619,308-107,263,478 , GRCh38.p12 chr14: 20,151,149-106,855,263 STXBP6, IGHG2, 1972 more genes
    nsv4355653copy number variation1nstd102humanPathogenic NCBI36 chr14: 92,077,081-104,401,040 , GRCh37.p13 chr14: 93,007,328-105,329,995 , GRCh38.p12 chr14: 92,540,983-104,863,658 ATP5MPL, SNORD114-6, 372 more genes
    nsv4355360copy number variation1nstd102humanPathogenic NCBI36 chr14: 83,448,442-106,334,665 , GRCh37.p13 chr14: 84,378,689-107,263,620 , GRCh38.p12 chr14: 83,912,345-106,855,405 SNORD114-17, RN7SL546P, 693 more genes
    nsv4355149copy number variation1nstd102humanPathogenic NCBI36 chr14: 103,320,848-106,349,815 , GRCh37.p13 chr14: 104,251,095-107,278,770 , GRCh38.p12 chr14: 103,784,758-106,870,558 SLC20A1P2, LOC107984670, 259 more genes
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