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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4684423copy number variation2nstd192human GRCh37 chr16: 28,859,861-29,044,746 , GRCh38.p12 chr16: 28,848,540-29,033,425 ATP2A1, CD19, 7 more genes
    nsv4684437copy number variation1nstd192human GRCh37 chr1: 146,501,347-147,825,662 , GRCh38.p12 chr1: 145,430,980-148,353,534 BCL9, FMO5, 106 more genes
    nsv4684426copy number variation1nstd192human GRCh37 chr1: 145,383,238-147,825,662 , GRCh38.p12 chr: NaN-NaN 0
    nsv4684449copy number variation1nstd192human GRCh37 chr3: 195,750,741-197,346,566 , GRCh38.p12 chr3: 196,023,870-197,619,695 BDH1, DLG1, 51 more genes
    nsv4684419copy number variation2nstd192human GRCh37 chr15: 30,927,361-32,514,341 , GRCh38.p12 chr15: 30,635,158-32,222,140 CHRNA7, TRPM1, 26 more genes
    nsv4684433copy number variation1nstd192human GRCh37 chr17: 34,815,551-36,375,180 , GRCh38.p12 chr17|NT_187614.1: 694,641-2,254,245 ACACA, LHX1, 45 more genes
    nsv4684435copy number variation1nstd192human GRCh37 chr1: 146,330,584-147,807,631 , GRCh38.p12 chr: NaN-NaN 0
    nsv4684432copy number variation1nstd192human GRCh37 chr17: 34,815,551-36,249,431 , GRCh38.p12 chr17: 36,459,737-37,889,809 , GRCh38.p12 chr17|NT_187614.1: 694,641-2,128,496 ACACA, LHX1, 36 more genes
    nsv4684425copy number variation6nstd192human GRCh37 chr16: 29,595,482-30,199,713 , GRCh38.p12 chr16: 29,584,161-30,188,392 ALDOA, CA5AP1, 39 more genes
    nsv4684445copy number variation1nstd192human GRCh38.p12 chr15: 23,452,228-28,285,036 , GRCh37 chr15: 23,697,375-28,530,182 GABRA5, GABRB3, 143 more genes
    nsv4684444copy number variation1nstd192human GRCh38.p12 chr15: 23,319,714-28,097,771 , GRCh37 chr15: 22,927,167-28,342,917 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 APBA2, CHRNA7, 258 more genes
    nsv4684443copy number variation1nstd192human GRCh38.p12 chr15: 23,319,714-27,732,633 , GRCh37 chr15: 22,853,785-27,977,779 GABRA5, GABRB3, 150 more genes
    nsv4684448copy number variation1nstd192human GRCh38.p12 chr1: 145,430,980-148,353,534 , GRCh37 chr1: 146,535,393-147,825,662 BCL9, FMO5, 106 more genes
    nsv4684438copy number variation1nstd192human GRCh38.p12 chr22: 18,339,130-21,114,846 , GRCh37 chr22: 18,892,574-21,469,135 ARVCF, COMT, 127 more genes
    nsv4684441copy number variation1nstd192human GRCh38.p12 chr22: 18,339,130-21,105,931 , GRCh37 chr22: 18,996,564-21,460,220 ARVCF, COMT, 126 more genes
    nsv4684440copy number variation1nstd192human GRCh38.p12 chr22: 18,339,130-21,105,931 , GRCh37 chr22: 18,924,955-21,460,220 ARVCF, COMT, 126 more genes
    nsv4684439copy number variation1nstd192human GRCh38.p12 chr22: 18,339,130-21,105,931 , GRCh37 chr22: 18,915,346-21,460,220 ARVCF, COMT, 126 more genes
    nsv4684417copy number variation2nstd192human GRCh38.p12 chr22: 18,339,130-21,105,931 , GRCh37 chr22: 18,892,574-21,460,220 ARVCF, COMT, 126 more genes
    nsv4684442copy number variation1nstd192human GRCh38.p12 chr22: 18,339,130-21,097,949 , GRCh37 chr22: 19,075,994-21,452,238 ARVCF, COMT, 125 more genes
    nsv4684427copy number variation1nstd192human GRCh38.p12 chr15: 30,647,899-32,222,900 , GRCh37 chr15: 30,940,102-32,515,101 CHRNA7, TRPM1, 26 more genes
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