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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7144944insertion1nstd232human GRCh37.p13 chr20: 57,002,518-57,002,518 , GRCh38.p12 chr20: 58,427,462-58,427,462 VAPB
    nsv7142774copy number variation1nstd232human GRCh37.p13 chr20: 56,989,012-56,989,187 , GRCh38.p12 chr20: 58,413,956-58,414,131 VAPB
    nsv7095798copy number variation1nstd102humanUncertain significance GRCh37 chr20: 57,009,638-57,019,291 , GRCh38.p12 chr20: 58,434,582-58,444,235 VAPB
    nsv7093587insertion1nstd102humanUncertain significance GRCh37 chr20: 57,009,638-57,009,638 , GRCh38 chr20: 58,434,582-58,434,582 VAPB
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7031120copy number variation1nstd229human GRCh38 chr20: 58,397,893-58,403,936 , GRCh37.p13 chr20: 56,972,949-56,978,992 VAPB
    nsv7023378copy number variation1nstd229human GRCh38 chr20: 58,420,990-58,421,091 , GRCh37.p13 chr20: 56,996,046-56,996,147 VAPB
    nsv7021617copy number variation1nstd229human GRCh38 chr20: 58,438,001-58,446,300 , GRCh37.p13 chr20: 57,013,057-57,021,356 VAPB
    nsv7021557copy number variation1nstd229human GRCh38 chr20: 58,430,670-58,526,355 , GRCh37.p13 chr20: 57,005,726-57,101,411 APCDD1L-DT, APCDD1L, 1 more genes
    nsv6551257copy number variation1nstd223human GRCh38 chr20: 58,386,022-58,387,687 , GRCh37.p13 chr20: 56,961,078-56,962,743 VAPB
    nsv6550073copy number variation1nstd223human GRCh38 chr20: 58,388,601-58,389,900 , GRCh37.p13 chr20: 56,963,657-56,964,956 VAPB
    nsv6537644copy number variation1nstd223human GRCh38 chr20: 58,428,612-58,429,933 , GRCh37.p13 chr20: 57,003,668-57,004,989 VAPB
    nsv6537321copy number variation1nstd223human GRCh38 chr20: 58,450,646-58,832,496 , GRCh37.p13 chr20: 57,025,702-57,407,551 STX16-NPEPL1, LOC107985410, 11 more genes
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
    nsv6314094copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,292,205-57,866,365 , GRCh38.p12 chr20: 56,717,149-59,291,310 PCK1, MIR296, 58 more genes
    nsv6311086copy number variation1nstd102humanUncertain significance GRCh37 chr20: 54,823,900-57,899,514 , GRCh38.p12 chr20: 56,248,844-59,324,459 CTSZ, SPO11, 75 more genes
    nsv6289075insertion2nstd214human GRCh38 chr20: 58,427,462-58,427,462 , GRCh37.p13 chr20: 57,002,518-57,002,518 VAPB
    nsv6285189insertion1nstd214human GRCh38 chr20: 58,427,483-58,427,483 , GRCh37.p13 chr20: 57,002,539-57,002,539 VAPB
    nsv6211858copy number variation1nstd214human GRCh38 chr20: 58,414,516-58,414,592 , GRCh37.p13 chr20: 56,989,572-56,989,648 VAPB
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