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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148135copy number variation1nstd102humanUncertain significance GRCh37 chr14: 57,675,327-59,806,898 , GRCh38.p12 chr14: 57,208,609-59,340,180 HMGB1P14, TOMM20L-DT, 36 more genes
    nsv7069510inversion1nstd229human GRCh38 chr14: 57,948,807-58,720,869 , GRCh37.p13 chr14: 58,415,525-59,187,587 RN7SL598P, TRK-CTT1-1, 19 more genes
    nsv7060499inversion1nstd229human GRCh38 chr14: 57,927,850-58,665,319 , GRCh37.p13 chr14: 58,394,568-59,132,037 TOMM20L, KIAA0586, 19 more genes
    nsv7060471inversion1nstd229human GRCh38 chr14: 54,671,401-63,742,041 , GRCh37.p13 chr14: 55,138,119-64,208,759 KTN1, OTX2-AS1, 153 more genes
    nsv6952443copy number variation1nstd229human GRCh38 chr14: 57,104,906-61,096,631 , GRCh37.p13 chr14: 57,571,624-61,563,349 LRRC9, RTN1, 71 more genes
    nsv6949728copy number variation1nstd229human GRCh38 chr14: 58,637,577-58,844,505 , GRCh37.p13 chr14: 59,104,295-59,311,223 LOC440181, LINC01500, 3 more genes
    nsv6949011copy number variation1nstd229human GRCh38 chr14: 57,104,849-61,096,728 , GRCh37.p13 chr14: 57,571,567-61,563,446 MAD2L1P1, AP5M1, 71 more genes
    nsv6944793copy number variation1nstd229human GRCh38 chr14: 58,648,757-58,654,089 , GRCh37.p13 chr14: 59,115,475-59,120,807 DACT1
    nsv6637688copy number variation1nstd102humanUncertain significance GRCh37 chr14: 58,833,909-59,109,480 , GRCh38.p12 chr14: 58,367,191-58,642,762 ARID4A, HNRNPCP1, 7 more genes
    nsv6637682copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 57,804,997-63,590,203 , GRCh38.p12 chr14: 57,338,279-63,123,485 PARP1P2, HIF1A, 91 more genes
    nsv6622787copy number variation1nstd224human GRCh37 chr14: 57,287,812-59,826,703 , GRCh38.p12 chr14: 56,821,094-59,359,985 KIAA0586, DAAM1, 41 more genes
    nsv6594267inversion1nstd223human GRCh38 chr14: 54,883,431-63,921,497 , GRCh37.p13 chr14: 55,350,149-64,388,215 RPL36AP1, GNRHR2P1, 152 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6258921mobile element insertion1nstd215human GRCh38 chr14: 58,643,052-58,643,052 , GRCh37.p13 chr14: 59,109,770-59,109,770 DACT1
    nsv6132878copy number variation1nstd213human GRCh37 chr14: 58,780,000-60,040,001 , GRCh38.p12 chr14: 58,313,282-59,573,283 TIMM9, L3HYPDH, 20 more genes
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5975448inversion1nstd209human GRCh38 chr14: 57,580,296-59,028,517 , GRCh37.p13 chr14: 58,047,014-59,495,235 PSMA3, ARID4A, 26 more genes
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5706073mobile element insertion1nstd211human GRCh38 chr14: 58,643,052-58,643,052 , GRCh37.p13 chr14: 59,109,770-59,109,770 DACT1
    nsv5427418mobile element insertion1nstd206human GRCh38 chr14: 58,643,052-58,643,103 , GRCh37.p13 chr14: 59,109,770-59,109,821 DACT1
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