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Items: 1 to 20 of 265

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099262copy number variation1nstd231human GRCh38.p12 chr1: 211,826,028-221,140,287 , GRCh37 chr1: 211,999,370-221,313,629 ATF3, CENPF, 114 more genes
    nsv7053240inversion1nstd229human GRCh38 chr1: 212,052,611-212,055,205 , GRCh37.p13 chr1: 212,225,953-212,228,547 DTL
    nsv7040987inversion1nstd229human GRCh38 chr1: 210,564,176-212,658,793 , GRCh37.p13 chr1: 210,737,520-212,832,135 LPGAT1, RFKP5, 44 more genes
    nsv6666858copy number variation1nstd229human GRCh38 chr1: 212,101,601-212,106,000 , GRCh37.p13 chr1: 212,274,943-212,279,342 DTL
    nsv6666485copy number variation1nstd229human GRCh38 chr1: 212,058,608-212,061,075 , GRCh37.p13 chr1: 212,231,950-212,234,417 DTL
    nsv6662971copy number variation1nstd229human GRCh38 chr1: 212,048,510-212,053,542 , GRCh37.p13 chr1: 212,221,852-212,226,884 RPL21P28, DTL
    nsv6660660copy number variation1nstd229human GRCh38 chr1: 212,085,655-212,089,180 , GRCh37.p13 chr1: 212,258,997-212,262,522 DTL
    nsv6660526copy number variation1nstd229human GRCh38 chr1: 212,091,883-212,096,185 , GRCh37.p13 chr1: 212,265,225-212,269,527 DTL
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6553852inversion1nstd223human GRCh38 chr1: 212,052,610-212,055,204 , GRCh37.p13 chr1: 212,225,952-212,228,546 DTL
    nsv6332912copy number variation1nstd223human GRCh38 chr1: 212,067,256-212,067,774 , GRCh37.p13 chr1: 212,240,598-212,241,116 DTL
    nsv6331485copy number variation1nstd223human GRCh38 chr1: 212,066,127-212,066,574 , GRCh37.p13 chr1: 212,239,469-212,239,916 DTL
    nsv6325553copy number variation1nstd223human GRCh38 chr1: 209,453,567-212,914,449 , GRCh37.p13 chr1: 209,626,912-213,087,791 ST13P19, RPS5P4, 74 more genes
    nsv6323962copy number variation1nstd223human GRCh38 chr1: 212,035,414-212,036,860 , GRCh37.p13 chr1: 212,208,756-212,210,202 INTS7, DTL
    nsv6323218copy number variation1nstd223human GRCh38 chr1: 212,056,501-212,058,700 , GRCh37.p13 chr1: 212,229,843-212,232,042 DTL
    nsv6317909copy number variation1nstd223human GRCh38 chr1: 212,058,607-212,061,074 , GRCh37.p13 chr1: 212,231,949-212,234,416 DTL
    nsv6294709mobile element insertion1nstd186human GRCh37 chr1: 212,245,164-212,245,215 , GRCh38.p12 chr1: 212,071,822-212,071,873 DTL
    nsv6133973copy number variation1nstd213human GRCh37 chr1: 212,030,000-212,280,001 , GRCh38.p12 chr1: 211,856,658-212,106,659 INTS7, DTL, 3 more genes
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