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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 MT1B, LOC105371293, 92 more genes
    nsv7094589copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228 SLC38A7, SETD6, 58 more genes
    nsv7069876inversion1nstd229human GRCh38 chr16: 58,076,774-64,694,512 , GRCh37.p13 chr16: 58,110,678-64,728,415 RN7SKP76, LOC105371311, 57 more genes
    nsv7069696inversion1nstd229human GRCh38 chr16: 58,205,688-64,165,972 , GRCh37.p13 chr16: 58,239,592-64,199,876 GOT2, RNU6-103P, 49 more genes
    nsv6987439copy number variation1nstd229human GRCh38 chr16: 58,314,411-58,441,509 , GRCh37.p13 chr16: 58,348,315-58,475,413 LINC02137, RNU6-269P, 2 more genes
    nsv6987321copy number variation1nstd229human GRCh38 chr16: 58,399,861-58,468,278 , GRCh37.p13 chr16: 58,433,765-58,502,182 NDRG4, LINC02137, 1 more genes
    nsv6981352copy number variation1nstd229human GRCh38 chr16: 58,404,314-58,407,706 , GRCh37.p13 chr16: 58,438,218-58,441,610 GINS3
    nsv6980844copy number variation1nstd229human GRCh38 chr16: 58,373,266-58,424,047 , GRCh37.p13 chr16: 58,407,170-58,457,951 GINS3, RNU6-269P, 2 more genes
    nsv6979498copy number variation1nstd229human GRCh38 chr16: 58,402,098-58,402,315 , GRCh37.p13 chr16: 58,436,002-58,436,219 GINS3
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6501461copy number variation1nstd223human GRCh38 chr16: 58,373,266-58,424,045 , GRCh37.p13 chr16: 58,407,170-58,457,949 LINC02137, RNU6-1110P, 2 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6120843copy number variation1nstd186human GRCh37 chr16: 58,429,850-58,430,797 , GRCh38.p12 chr16: 58,395,946-58,396,893 GINS3
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv6082730insertion1nstd212human GRCh38 chr16: 58,395,903-58,395,903 , GRCh37.p13 chr16: 58,429,807-58,429,807 GINS3
    nsv6037940copy number variation1nstd212human GRCh38 chr16: 58,396,543-58,396,690 , GRCh37.p13 chr16: 58,430,447-58,430,594 GINS3
    nsv6034541copy number variation1nstd212human GRCh38 chr16: 58,396,195-58,396,317 , GRCh37.p13 chr16: 58,430,099-58,430,221 GINS3
    nsv6027251copy number variation1nstd212human GRCh38 chr16: 58,396,992-58,397,044 , GRCh37.p13 chr16: 58,430,896-58,430,948 GINS3
    nsv6024558copy number variation1nstd212human GRCh38 chr16: 58,395,928-58,396,233 , GRCh37.p13 chr16: 58,429,832-58,430,137 GINS3
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