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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095026copy number variation2nstd102humanUncertain significance GRCh37 chr16: 49,525,186-51,631,253 , GRCh38.p12 chr16: 49,491,275-51,597,342 RNA5SP426, RPL34P29, 35 more genes
    nsv6982398copy number variation1nstd229human GRCh38 chr16: 49,432,901-50,109,800 , GRCh37.p13 chr16: 49,466,812-50,143,711 CNEP1R1, ADAM3B, 10 more genes
    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
    nsv6634436copy number variation1nstd102humanassociation GRCh37 chr16: 50,089,192-51,652,287 , GRCh38.p12 chr16: 50,055,281-51,618,376 CYLD-AS1, LOC107984892, 29 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
    nsv6250262mobile element insertion1nstd215human GRCh38 chr16: 50,097,317-50,097,317 , GRCh37.p13 chr16: 50,131,228-50,131,228 RNY4P3, HEATR3
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    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
    nsv5358177translocation1nstd200human GRCh38 chr16: 50,096,747-50,096,747 , GRCh38 chr16: 50,097,960-50,097,960 , GRCh37.p13 chr16: 50,130,658-50,130,658 , GRCh37.p13 chr16: 50,131,871-50,131,871 RNY4P3, HEATR3
    nsv5005666copy number variation1nstd200human GRCh38 chr16: 50,096,515-50,097,951 , GRCh37.p13 chr16: 50,130,426-50,131,862 RNY4P3, HEATR3
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4456728copy number variation1nstd102humanUncertain significance GRCh37 chr16: 49,966,361-50,215,920 , GRCh38.p12 chr16: 49,932,450-50,182,009 RPL34P29, TENT4B, 6 more genes
    nsv4365843copy number variation1nstd173human GRCh37 chr16: 46,464,489-55,795,214 , GRCh38.p12 chr16: 46,430,577-55,761,302 , LOC100526838, 158 more genes
    nsv4365186copy number variation1nstd173human GRCh37 chr16: 46,503,205-57,376,253 , GRCh38.p12 chr16: 46,469,293-57,342,341 , TOX3, 210 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
    nsv3920484copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,466,829-51,673,196 , GRCh37 chr16: 46,500,741-51,707,107 , NCBI36 chr16: 45,058,242-50,264,608 NETO2, LOC100130180, 92 more genes
    nsv3918521copy number variation1nstd102humanPathogenic NCBI36 chr16: 48,276,933-66,993,116 , GRCh37 chr16: 49,719,432-68,435,615 , GRCh38 chr16: 49,685,521-68,401,712 CYLD-AS2, MT1F, 342 more genes
    nsv3917427copy number variation1nstd102humanBenign NCBI36 chr16: 32,529,496-88,822,254 , GRCh37.p13 chr16: 32,621,995-90,294,753 , GRCh38.p12 chr16: 32,610,674-90,228,345 TXNL4B, KLHL36, 968 more genes
    nsv3917348copy number variation1nstd102humanPathogenic NCBI36 chr16: 48,332,219-50,468,032 , GRCh37 chr16: 49,774,718-51,910,531 , GRCh38 chr16: 49,740,807-51,876,620 NOD2, LOC105371256, 38 more genes
    nsv3917177copy number variation1nstd102humanPathogenic GRCh38 chr16: 49,570,553-53,467,065 , NCBI36 chr16: 48,161,965-52,058,478 , GRCh37 chr16: 49,604,464-53,500,977 LOC107984901, LOC100288763, 66 more genes
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