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Items: 1 to 20 of 6690

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145324copy number variation1nstd232human GRCh37.p13 chr10: 56,066,781-56,066,840 , GRCh38.p12 chr10: 54,307,021-54,307,080 PCDH15
    nsv7144898insertion1nstd232human GRCh37.p13 chr10: 56,539,257-56,539,257 , GRCh38.p12 chr10: 54,779,497-54,779,497 PCDH15
    nsv7140621copy number variation1nstd232human GRCh37.p13 chr10: 57,298,383-57,298,499 , GRCh38.p12 chr10: 55,538,623-55,538,739 PCDH15
    nsv7140077insertion1nstd232human GRCh37.p13 chr10: 56,762,358-56,762,358 , GRCh38.p12 chr10: 55,002,598-55,002,598 PCDH15
    nsv7138825copy number variation1nstd232human GRCh37.p13 chr10: 56,066,779-56,066,840 , GRCh38.p12 chr10: 54,307,019-54,307,080 PCDH15
    nsv7138057copy number variation1nstd232human GRCh37.p13 chr10: 55,725,740-55,725,827 , GRCh38.p12 chr10: 53,965,980-53,966,067 PCDH15
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093880copy number variation1nstd102humanPathogenic GRCh37 chr10: 55,826,507-56,424,032 , GRCh38.p12 chr10: 54,066,747-54,664,272 NEFMP1, PCDH15, 3 more genes
    nsv7093879copy number variation1nstd102humanPathogenic GRCh37 chr10: 55,755,399-56,424,032 , GRCh38.p12 chr10: 53,995,639-54,664,272 PCDH15, RNU6-687P, 3 more genes
    nsv7093878copy number variation1nstd102humanUncertain significance GRCh37 chr10: 55,698,555-55,698,735 , GRCh38.p12 chr10: 53,938,795-53,938,975 PCDH15
    nsv7093792copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 56,077,021-56,138,712 , GRCh38.p12 chr10: 54,317,261-54,378,952 PCDH15
    nsv7093791copy number variation1nstd102humanPathogenic GRCh37 chr10: 55,849,734-55,849,833 , GRCh38.p12 chr10: 54,089,974-54,090,073 PCDH15
    nsv7093717copy number variation1nstd102humanPathogenic GRCh37 chr10: 55,912,840-55,913,073 , GRCh38.p12 chr10: 54,153,080-54,153,313 PCDH15
    nsv7093716copy number variation1nstd102humanPathogenic GRCh37 chr10: 55,826,507-56,106,254 , GRCh38.p12 chr10: 54,066,747-54,346,494 PCDH15
    nsv7093639copy number variation1nstd102humanPathogenic GRCh37 chr10: 56,287,562-56,288,172 , GRCh38.p12 chr10: 54,527,802-54,528,412 LOC105378311, PCDH15
    nsv7093638copy number variation1nstd102humanPathogenic GRCh37 chr10: 56,106,115-56,106,254 , GRCh38.p12 chr10: 54,346,355-54,346,494 PCDH15
    nsv7093637copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 55,892,683-55,893,842 , GRCh38.p12 chr10: 54,132,923-54,134,082 PCDH15
    nsv7093636copy number variation1nstd102humanPathogenic GRCh37 chr10: 55,698,565-55,700,745 , GRCh38.p12 chr10: 53,938,805-53,940,985 PCDH15
    nsv7093449delins1nstd102humanPathogenic GRCh37 chr10: 55,943,214-55,943,233 , GRCh38 chr10: 54,183,454-54,183,473 PCDH15
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