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Items: 11

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    Number of Variants: 11

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6624560copy number variation4nstd224human GRCh37 chr18: 4,462,824-4,488,582 , GRCh38.p12 chr18: 4,462,824-4,488,582 ELOCP27
    nsv6625477copy number variation6nstd224human GRCh37 chr1: 106,026,464-106,089,142 , GRCh38.p12 chr1: 105,483,842-105,546,520 LOC105378881
    nsv6630667copy number variation1nstd224human GRCh37 chr6: 136,582,458-136,599,544 , GRCh38.p12 chr6: 136,261,320-136,278,406 BCLAF1
    nsv6627024copy number variation1nstd224human GRCh37 chr21: 47,546,061-47,556,936 , GRCh38.p12 chr21: 46,126,147-46,137,022 FTCD, COL6A2
    nsv6623757copy number variation4nstd224human GRCh37 chr16: 75,564,172-75,577,559 , GRCh38.p12 chr16: 75,530,274-75,543,661 CHST5, TMEM231
    nsv6631410copy number variation7nstd224human GRCh37 chr6: 35,754,822-35,765,043 , GRCh38.p12 chr6: 35,787,045-35,797,266 CLPSL1, CLPS
    nsv6625614copy number variation1nstd224human GRCh37 chr1: 12,880,153-12,921,311 , GRCh38.p12 chr1: 12,820,291-12,861,456 , GRCh38.p12 chr1|NW_012132914.1: 1,804-42,969 LINC01784, HNRNPCL1, 3 more genes
    nsv6625429copy number variation88nstd224human GRCh37 chr19: 54,731,679-54,742,965 , GRCh38.p12 chr19: 54,227,805-54,239,089 , GRCh38.p12 chr19|NT_187693.1: 202,793-214,079 , GRCh38.p12 chr19|NW_003571060.1: 202,792-214,078 , GRCh38.p12 chr19|NW_003571054.1: 202,605-213,862 LILRA6, LOC107985279, 1 more genes
    nsv6622655copy number variation56nstd224human GRCh37 chr14: 45,181,337-45,224,071 , GRCh38.p12 chr14: 44,712,134-44,754,868 0
    nsv6630221copy number variation102nstd224human GRCh37 chr5: 113,160,490-113,171,928 , GRCh38.p12 chr5: 113,824,793-113,836,231 0
    nsv6622449copy number variation16nstd224human GRCh37 chr14: 20,216,352-20,420,151 , GRCh38.p12 chr14: 19,748,193-19,951,992 OR4K1, OR4M1, 10 more genes
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