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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970807insertion1nstd209human GRCh38 chr19: 4,411,597-4,411,597 , GRCh37.p13 chr19: 4,411,594-4,411,594 , CHAF1A
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5645295insertion1nstd207human GRCh38 chr19: 4,408,461-4,408,461 , GRCh37.p13 chr19: 4,408,458-4,408,458 CHAF1A
    nsv5518650copy number variation1nstd206human GRCh38 chr19: 4,441,070-4,441,190 , GRCh37.p13 chr19: 4,441,067-4,441,187 CHAF1A
    nsv5320848copy number variation1nstd204human GRCh38.p13 chr19: 4,440,840-4,449,997 , GRCh37.p13 chr19: 4,440,837-4,449,994 MIR4746, CHAF1A, 1 more genes
    nsv5320552copy number variation1nstd204human GRCh38.p13 chr19: 4,418,997-4,419,557 , GRCh37.p13 chr19: 4,418,994-4,419,554 CHAF1A
    nsv5299582copy number variation1nstd204human GRCh37.p13 chr19: 4,335,098-4,420,197 , GRCh38.p13 chr19: 4,335,101-4,420,200 , SH3GL1, 4 more genes
    nsv5292942copy number variation1nstd204human GRCh38.p13 chr19: 4,440,888-4,449,939 , GRCh37.p13 chr19: 4,440,885-4,449,936 UBXN6, MIR4746, 1 more genes
    nsv5292408copy number variation1nstd204human GRCh38.p13 chr19: 2,552,101-4,875,100 , GRCh37.p13 chr19: 2,552,099-4,875,112 , S1PR4, 93 more genes
    nsv5292334copy number variation1nstd204human GRCh38.p13 chr19: 4,425,006-4,427,880 , GRCh37.p13 chr19: 4,425,003-4,427,877 CHAF1A
    nsv5288993copy number variation1nstd204human GRCh38.p13 chr19: 4,398,548-4,402,093 , GRCh37.p13 chr19: 4,398,545-4,402,090 CHAF1A, SH3GL1
    nsv5284500copy number variation1nstd204human GRCh38.p13 chr19: 4,068,001-4,541,200 , GRCh37.p13 chr19: 4,067,999-4,541,212 , EIF1P6, 20 more genes
    nsv5167960mobile element insertion1nstd203human GRCh38 chr19: 4,413,373-4,413,384 , GRCh37.p13 chr19: 4,413,370-4,413,381 , CHAF1A
    nsv4864846copy number variation1nstd200human GRCh37 chr19: 4,440,843-4,449,991 , GRCh38.p12 chr19: 4,440,846-4,449,994 MIR4746, CHAF1A, 1 more genes
    nsv4852664copy number variation1nstd200human GRCh37 chr19: 4,441,067-4,441,187 , GRCh38.p12 chr19: 4,441,070-4,441,190 CHAF1A
    nsv4652040copy number variation1nstd186human GRCh37 chr19: 4,399,000-4,404,575 , GRCh38.p12 chr19: 4,399,003-4,404,578 SH3GL1, CHAF1A
    nsv4514022mobile element insertion1nstd166human GRCh37.p13 chr19: 4,414,628-4,414,628 , GRCh38.p12 chr19: 4,414,631-4,414,631 CHAF1A
    nsv4513836mobile element insertion1nstd166human GRCh37.p13 chr19: 4,438,513-4,438,513 , GRCh38.p12 chr19: 4,438,516-4,438,516 CHAF1A
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
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