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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947288copy number variation1nstd209human GRCh38 chr14: 76,171,166-76,171,311 , GRCh37.p13 chr14: 76,637,509-76,637,654 GPATCH2L
    nsv5931678copy number variation1nstd209human GRCh38 chr14: 75,925,125-77,416,814 , GRCh37.p13 chr14: 76,391,468-77,883,157 TMED8, LOC105370573, 37 more genes
    nsv5716533mobile element insertion1nstd211human GRCh38 chr14: 76,174,308-76,174,308 , GRCh37.p13 chr14: 76,640,651-76,640,651 GPATCH2L
    nsv5708055mobile element insertion1nstd211human GRCh38 chr14: 76,204,599-76,204,599 , GRCh37.p13 chr14: 76,670,942-76,670,942 GPATCH2L
    nsv5564102mobile element insertion1nstd206human GRCh38 chr14: 76,174,323-76,174,359 , GRCh37.p13 chr14: 76,640,666-76,640,702 GPATCH2L
    nsv5414790mobile element insertion1nstd206human GRCh38 chr14: 76,204,599-76,204,650 , GRCh37.p13 chr14: 76,670,942-76,670,993 GPATCH2L
    nsv5357407translocation1nstd200human GRCh38 chr14: 76,173,955-76,173,955 , GRCh38 chr14: 76,174,249-76,174,249 , GRCh37.p13 chr14: 76,640,298-76,640,298 , GRCh37.p13 chr14: 76,640,592-76,640,592 GPATCH2L
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4832459copy number variation1nstd200human GRCh37 chr14: 76,666,216-76,666,294 , GRCh38.p12 chr14: 76,199,873-76,199,951 GPATCH2L
    nsv4513806mobile element insertion1nstd166human GRCh37.p13 chr14: 76,659,568-76,659,568 , GRCh38.p12 chr14: 76,193,225-76,193,225 GPATCH2L
    nsv4510741mobile element insertion1nstd166human GRCh37.p13 chr14: 76,672,266-76,672,266 , GRCh38.p12 chr14: 76,205,923-76,205,923 GPATCH2L
    nsv4506851mobile element insertion1nstd166human GRCh37.p13 chr14: 76,645,272-76,645,272 , GRCh38.p12 chr14: 76,178,929-76,178,929 GPATCH2L
    nsv4504120mobile element insertion1nstd166human GRCh37.p13 chr14: 76,633,723-76,633,723 , GRCh38.p12 chr14: 76,167,380-76,167,380 GPATCH2L
    nsv3924066copy number variation1nstd102humanUncertain significance GRCh37 chr14: 75,452,898-76,865,601 , GRCh38 chr14: 74,986,195-76,399,258 , NCBI36 chr14: 74,522,651-75,935,354 RPS24P2, EIF2B2, 29 more genes
    nsv3923727copy number variation1nstd102humanPathogenic GRCh37 chr14: 70,028,816-82,441,728 , GRCh38 chr14: 69,562,099-81,975,384 , NCBI36 chr14: 69,098,569-81,511,481 CEP128, COX6CP11, 240 more genes
    nsv3923448copy number variation1nstd102humanPathogenic NCBI36 chr14: 73,413,528-77,578,518 , GRCh38 chr14: 73,877,072-78,042,422 , GRCh37 chr14: 74,343,775-78,508,765 ZC2HC1C, RPL21P10, 113 more genes
    nsv3922441copy number variation1nstd102humanPathogenic GRCh38 chr14: 75,489,052-79,610,332 , GRCh37 chr14: 75,955,395-80,076,675 , NCBI36 chr14: 75,025,148-79,146,428 IRF2BPL, LOC105370583, 69 more genes
    nsv3922094copy number variation1nstd102humanPathogenic GRCh38 chr14: 73,655,772-106,879,298 , GRCh37 chr14: 74,122,475-107,287,505 , NCBI36 chr14: 73,192,228-106,358,550 LOC105370614, LOC105370617, 849 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3919051copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 72,879,674-78,371,155 , GRCh37 chr14: 73,809,921-79,301,402 , GRCh38 chr14: 73,343,213-78,835,059 ACYP1, ENTPD5, 137 more genes
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