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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968372insertion1nstd209human GRCh37.p13 chr11: 74,064,908-74,064,908 , GRCh38 chr11: 74,353,863-74,353,863 PGM2L1, HNRNPA1P40, 1 more genes
    nsv5646359insertion1nstd207human GRCh38 chr11: 74,353,863-74,353,863 , GRCh37.p13 chr11: 74,064,908-74,064,908 PGM2L1, HNRNPA1P40, 1 more genes
    nsv5544506insertion1nstd206human GRCh38 chr11: 74,353,870-74,353,913 , GRCh37.p13 chr11: 74,064,915-74,064,958 PGM2L1, HNRNPA1P40, 1 more genes
    nsv5494028copy number variation1nstd206human GRCh38 chr11: 74,225,600-74,828,943 , GRCh37.p13 chr11: 73,936,645-74,539,988 RNF169, MIR4696, 19 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5136814mobile element insertion1nstd203human GRCh38 chr11: 74,355,540-74,355,553 , GRCh37.p13 chr11: 74,066,585-74,066,598 PGM2L1, HNRNPA1P40, 1 more genes
    nsv5128516mobile element insertion1nstd203human GRCh38 chr11: 74,355,518-74,355,553 , GRCh37.p13 chr11: 74,066,563-74,066,598 PGM2L1, HNRNPA1P40, 1 more genes
    nsv5120809mobile element insertion1nstd203human GRCh38 chr11: 74,355,553-74,355,567 , GRCh37.p13 chr11: 74,066,598-74,066,612 PGM2L1, HNRNPA1P40, 1 more genes
    nsv4767004insertion1nstd199human GRCh37 chr11: 74,064,908-74,064,908 , GRCh38.p12 chr11: 74,353,863-74,353,863 PGM2L1, HNRNPA1P40, 1 more genes
    nsv4446391insertion1nstd175human GRCh37 chr11: 74,064,905-74,064,905 , GRCh38.p12 chr11: 74,353,860-74,353,860 PGM2L1, HNRNPA1P40, 1 more genes
    nsv4418797copy number variation1nstd174human GRCh37 chr11: 73,936,645-74,539,988 , GRCh38.p12 chr11: 74,225,600-74,828,943 POLD3, CHRDL2, 19 more genes
    nsv3929188insertion1nstd167human GRCh37 chr11: 74,064,907-74,064,907 , GRCh38.p12 chr11: 74,353,862-74,353,862 PGM2L1, HNRNPA1P40, 1 more genes
    nsv3916301copy number variation1nstd102humanPathogenic GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216 RN7SL786P, LIPT2-AS1, 146 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 SESN3, LOC107984352, 694 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3559702insertion3nstd152human GRCh38 chr11: 74,353,847-74,353,877 , GRCh37.p13 chr11: 74,064,892-74,064,922 PGM2L1, HNRNPA1P40, 1 more genes
    nsv3333670insertion14nstd162human GRCh38 chr11: 74,353,864-74,353,864 , GRCh37.p13 chr11: 74,064,909-74,064,909 PGM2L1, HNRNPA1P40, 1 more genes
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