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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5931660copy number variation1nstd209human GRCh38 chr16: 5,029,297-5,029,347 , GRCh37.p13 chr16: 5,079,298-5,079,348 NAGPA
    nsv5587762copy number variation1nstd207human GRCh38 chr16: 5,029,297-5,029,347 , GRCh37.p13 chr16: 5,079,298-5,079,348 NAGPA
    nsv5529697copy number variation1nstd206human GRCh38 chr16: 4,957,857-5,308,524 , GRCh37.p13 chr16: 5,007,858-5,358,525 , LOC105371067, 12 more genes
    nsv5527611copy number variation1nstd206human GRCh38 chr16: 5,004,687-5,310,668 , GRCh37.p13 chr16: 5,054,688-5,360,669 , RPS3AP48, 12 more genes
    nsv5525042copy number variation1nstd206human GRCh38 chr16: 5,029,297-5,029,348 , GRCh37.p13 chr16: 5,079,298-5,079,349 NAGPA
    nsv5349444translocation1nstd200human GRCh38 chr16: 5,026,222-5,026,222 , GRCh38 chr16: 5,026,082-5,026,082 , GRCh37.p13 chr16: 5,076,083-5,076,083 , GRCh37.p13 chr16: 5,076,223-5,076,223 NAGPA
    nsv5313629copy number variation1nstd204human GRCh38.p13 chr16: 4,957,847-5,308,533 , GRCh37.p13 chr16: 5,007,848-5,358,534 , SEC14L5, 12 more genes
    nsv5269327copy number variation1nstd204human GRCh37.p13 chr16: 5,008,302-5,252,801 , GRCh38.p13 chr16: 4,958,301-5,202,800 SEC14L5, NAGPA, 6 more genes
    nsv5264822copy number variation1nstd204human GRCh38.p13 chr16: 5,028,990-5,032,239 , GRCh37.p13 chr16: 5,078,991-5,082,240 NAGPA, NAGPA-AS1
    nsv5008116copy number variation1nstd200human GRCh38 chr16: 4,732,537-5,127,796 , GRCh37.p13 chr16: 4,782,538-5,177,797 NAGPA, PPL, 16 more genes
    nsv4994362copy number variation1nstd200human GRCh38 chr16: 5,015,039-5,054,725 , GRCh37.p13 chr16: 5,065,040-5,104,726 NAGPA, C16orf89, 2 more genes
    nsv4994361copy number variation1nstd200human GRCh38 chr16: 5,004,687-5,310,668 , GRCh37.p13 chr16: 5,054,688-5,360,669 , SEC14L5, 12 more genes
    nsv4994360copy number variation1nstd200human GRCh38 chr16: 4,957,857-5,308,524 , GRCh37.p13 chr16: 5,007,858-5,358,525 , RPS3AP48, 12 more genes
    nsv4994358copy number variation1nstd200human GRCh38 chr16: 4,924,814-5,845,027 , GRCh37.p13 chr16: 4,974,815-5,895,028 , LOC107984828, 17 more genes
    nsv4854362copy number variation1nstd200human GRCh37 chr16: 5,065,040-5,104,726 , GRCh38.p12 chr16: 5,015,039-5,054,725 SEC14L5, C16orf89, 2 more genes
    nsv4854361copy number variation1nstd200human GRCh37 chr16: 5,054,688-5,360,669 , GRCh38.p12 chr16: 5,004,687-5,310,668 , ENPP7P14, 12 more genes
    nsv4854360copy number variation1nstd200human GRCh37 chr16: 5,007,858-5,358,525 , GRCh38.p12 chr16: 4,957,857-5,308,524 , RBFOX1, 12 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
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