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Items: 1 to 20 of 88

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5506599copy number variation1nstd206human GRCh38 chr14: 92,986,904-93,282,458 , GRCh37.p13 chr14: 93,453,249-93,748,804 BTBD7, RPL18AP1, 8 more genes
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5004941copy number variation1nstd200human GRCh38 chr14: 93,064,744-93,074,532 , GRCh37.p13 chr14: 93,531,089-93,540,877 ITPK1, ITPK1-AS1
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 SHLD2P2, RPL15P2, 175 more genes
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4322697inversion1nstd166human GRCh37.p13 chr14: 93,328,296-94,706,279 , GRCh38.p12 chr14: 92,861,951-94,140,555 , GRCh38.p12 chr14|NT_187601.1: 1-1,354,504 ASB2, UNC79, 29 more genes
    nsv3962429insertion1nstd168human GRCh38 chr14: 93,069,233-93,108,516 , GRCh37.p13 chr14: 93,535,578-93,574,861 ITPK1, ITPK1-AS1
    nsv3922566copy number variation1nstd102humanPathogenic GRCh38 chr14: 90,255,156-95,274,696 , GRCh37 chr14: 90,721,500-95,741,033 , NCBI36 chr14: 89,791,253-94,810,786 RPSAP4, LOC105370622, 97 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
    nsv3921292copy number variation1nstd102humanPathogenic GRCh38 chr14: 91,455,861-106,832,642 , GRCh37 chr14: 91,922,205-107,240,869 , NCBI36 chr14: 90,991,958-106,311,914 IGHVII-15-1, LINC03117, 594 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
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv3915681copy number variation1nstd102humanPathogenic NCBI36 chr14: 76,758,891-106,358,550 , GRCh37 chr14: 77,689,138-107,287,505 , GRCh38 chr14: 77,222,795-106,879,298 IGHV3-32, SNORD114-31, 751 more genes
    nsv3914983copy number variation1nstd102humanPathogenic GRCh38 chr14: 86,094,030-106,832,642 , GRCh37 chr14: 86,560,374-107,240,869 , NCBI36 chr14: 85,630,127-106,311,914 IGHD5-5, EML5, 658 more genes
    nsv3914883copy number variation1nstd102humanPathogenic NCBI36 chr14: 92,077,081-104,401,040 , GRCh37 chr14: 93,007,328-105,329,995 , GRCh38 chr14: 92,540,983-104,863,658 LINC03117, EIF5, 360 more genes
    nsv3914418copy number variation1nstd102humanPathogenic NCBI36 chr14: 92,401,537-106,360,585 , GRCh37.p13 chr14: 93,331,784-107,289,540 , GRCh38.p12 chr14: 92,865,439-106,881,350 IGHVII-60-1, ATG2B, 582 more genes
    nsv3913232copy number variation1nstd102humanUncertain significance NCBI36 chr14: 92,205,048-92,687,955 , GRCh37.p13 chr14: 93,135,295-93,618,202 , GRCh38.p12 chr14: 92,885,439-93,151,857 , GRCh38.p12 chr14|NT_187601.1: 1-266,419 ITPK1, LINC02833, 4 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 BANF1P1, IGHV1-68, 1996 more genes
    nsv3905673copy number variation1nstd102humanUncertain significance GRCh37 chr14: 93,498,930-96,059,698 , GRCh38.p12 chr14|NT_187601.1: 147,147-1,475,710 , GRCh38.p12 chr14: 93,207,711-95,593,361 GON7, LOC107984710, 65 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 CRIP1, GPATCH2L, 1929 more genes
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