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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5933382copy number variation1nstd209human GRCh38 chr14: 58,252,948-58,253,021 , GRCh37.p13 chr14: 58,719,666-58,719,739 PSMA3
    nsv5649292insertion1nstd207human GRCh38 chr14: 58,254,340-58,254,340 , GRCh37.p13 chr14: 58,721,058-58,721,058 PSMA3
    nsv5502482copy number variation1nstd206human GRCh38 chr14: 58,269,196-58,269,430 , GRCh37.p13 chr14: 58,735,914-58,736,148 PSMA3-AS1, PSMA3
    nsv5263141copy number variation1nstd204human GRCh38.p13 chr14: 58,244,300-58,246,749 , GRCh37.p13 chr14: 58,711,018-58,713,467 PSMA3
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4756566insertion1nstd199human GRCh37 chr14: 58,721,058-58,721,058 , GRCh38.p12 chr14: 58,254,340-58,254,340 PSMA3
    nsv4742004copy number variation1nstd199human GRCh37 chr14: 58,715,381-58,715,447 , GRCh38.p12 chr14: 58,248,663-58,248,729 PSMA3
    nsv4676003copy number variation1nstd102humanUncertain significance GRCh37 chr14: 58,735,449-58,853,507 , GRCh38.p12 chr14: 58,268,731-58,386,789 ARID4A, HMGB1P14, 5 more genes
    nsv4674918copy number variation1nstd102humanPathogenic GRCh37 chr14: 56,605,398-59,404,256 , GRCh38.p12 chr14: 56,138,680-58,937,538 RNU6-1204P, LOC440180, 42 more genes
    nsv4575653mobile element insertion1nstd166human GRCh37.p13 chr14: 58,734,393-58,734,393 , GRCh38.p12 chr14: 58,267,675-58,267,675 PSMA3-AS1, PSMA3
    nsv4366653copy number variation1nstd173human GRCh37 chr14: 58,725,316-58,772,018 , GRCh38.p12 chr14: 58,258,598-58,305,300 HMGB1P14, PSMA3-AS1, 4 more genes
    nsv4220354copy number variation1nstd166human GRCh37.p13 chr14: 58,730,842-58,731,214 , GRCh38.p12 chr14: 58,264,124-58,264,496 PSMA3-AS1, PSMA3
    nsv4218378copy number variation1nstd166human GRCh37.p13 chr14: 58,715,416-58,715,498 , GRCh38.p12 chr14: 58,248,698-58,248,780 PSMA3
    nsv4217894copy number variation1nstd166human GRCh37.p13 chr14: 58,712,210-58,713,450 , GRCh38.p12 chr14: 58,245,492-58,246,732 PSMA3
    nsv3930503insertion1nstd167human GRCh37 chr14: 58,721,058-58,721,058 , GRCh38.p12 chr14: 58,254,340-58,254,340 PSMA3
    nsv3924033copy number variation1nstd102humanPathogenic GRCh37 chr14: 58,120,131-64,560,246 , GRCh38 chr14: 57,653,413-64,093,528 , NCBI36 chr14: 57,189,884-63,629,999 DACT1, UBA52P3, 105 more genes
    nsv3922652copy number variation1nstd102humanPathogenic GRCh37 chr14: 57,507,754-67,674,948 , NCBI36 chr14: 56,577,507-66,744,701 , GRCh38 chr14: 57,041,036-67,208,231 PARP1P2, SNAPC1, 160 more genes
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