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Items: 1 to 20 of 325

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138232copy number variation1nstd232human GRCh37.p13 chr6: 44,149,354-44,149,478 , GRCh38.p12 chr6: 44,181,617-44,181,741 CAPN11
    nsv7097331copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,162,409-44,154,249 , GRCh38.p12 chr6: 42,194,671-44,186,512 MRPS10, CUL9, 70 more genes
    nsv6794808copy number variation1nstd229human GRCh38 chr6: 44,157,801-44,160,100 , GRCh37.p13 chr6: 44,125,538-44,127,837 CAPN11, LOC107986599
    nsv6791974copy number variation1nstd229human GRCh38 chr6: 44,149,931-44,182,023 , GRCh37.p13 chr6: 44,117,668-44,149,760 LOC107986599, TMEM63B, 1 more genes
    nsv6791553copy number variation1nstd229human GRCh38 chr6: 44,159,900-44,160,344 , GRCh37.p13 chr6: 44,127,637-44,128,081 CAPN11
    nsv6789812copy number variation1nstd229human GRCh38 chr6: 44,178,301-44,185,000 , GRCh37.p13 chr6: 44,146,038-44,152,737 CAPN11, LOC105375072
    nsv6787193copy number variation1nstd229human GRCh38 chr6: 44,181,401-44,326,600 , GRCh37.p13 chr6: 44,149,138-44,294,337 TMEM151B, AARS2, 10 more genes
    nsv6636332copy number variation1nstd102humanUncertain significance GRCh37 chr6: 43,571,555-44,154,599 , GRCh38.p12 chr6: 43,603,818-44,186,862 CAPN11, LOC105375068, 18 more genes
    nsv6631062copy number variation1nstd224human GRCh37 chr6: 44,138,947-44,151,490 , GRCh38.p12 chr6: 44,171,210-44,183,753 CAPN11
    nsv6566770inversion1nstd223human GRCh38 chr6: 42,194,666-44,186,502 , GRCh37.p13 chr6: 42,162,404-44,154,239 RPL36AP5, MIR6780B, 70 more genes
    nsv6414436copy number variation1nstd223human GRCh38 chr6: 44,168,359-44,168,840 , GRCh37.p13 chr6: 44,136,096-44,136,577 CAPN11
    nsv6413593copy number variation1nstd223human GRCh38 chr6: 44,178,285-44,185,029 , GRCh37.p13 chr6: 44,146,022-44,152,766 CAPN11, LOC105375072
    nsv6408894copy number variation1nstd223human GRCh38 chr6: 44,173,132-44,178,247 , GRCh37.p13 chr6: 44,140,869-44,145,984 CAPN11
    nsv6405404copy number variation1nstd223human GRCh38 chr6: 44,157,101-44,159,900 , GRCh37.p13 chr6: 44,124,838-44,127,637 CAPN11, LOC107986599
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6302310copy number variation1nstd186human GRCh37 chr6: 44,128,985-44,151,548 , GRCh38.p12 chr6: 44,161,248-44,183,811 CAPN11
    nsv6280187insertion1nstd214human GRCh38 chr6: 44,181,434-44,181,434 , GRCh37.p13 chr6: 44,149,171-44,149,171 CAPN11
    nsv6179712copy number variation1nstd214human GRCh38 chr6: 44,181,494-44,181,573 , GRCh37.p13 chr6: 44,149,231-44,149,310 CAPN11
    nsv6178215copy number variation1nstd214human GRCh38 chr6: 44,181,496-44,181,573 , GRCh37.p13 chr6: 44,149,233-44,149,310 CAPN11
    nsv6177304copy number variation1nstd214human GRCh38 chr6: 44,182,206-44,182,283 , GRCh37.p13 chr6: 44,149,943-44,150,020 CAPN11
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