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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5928982copy number variation1nstd209human GRCh38 chr12: 111,422,669-111,429,435 , GRCh37.p13 chr12: 111,860,473-111,867,239 SH2B3
    nsv5864396copy number variation2nstd209human GRCh38 chr12: 111,426,906-111,428,005 , GRCh37.p13 chr12: 111,864,710-111,865,809 SH2B3
    nsv5862785copy number variation1nstd209human GRCh38 chr12: 111,425,206-111,429,560 , GRCh37.p13 chr12: 111,863,010-111,867,364 SH2B3
    nsv5860252copy number variation2nstd209human GRCh38 chr12: 111,423,306-111,424,305 , GRCh37.p13 chr12: 111,861,110-111,862,109 SH2B3
    nsv5849327copy number variation2nstd209human GRCh38 chr12: 111,422,606-111,423,705 , GRCh37.p13 chr12: 111,860,410-111,861,509 SH2B3
    nsv5848593copy number variation1nstd209human GRCh38 chr12: 111,422,607-111,426,205 , GRCh37.p13 chr12: 111,860,411-111,864,009 SH2B3
    nsv5707518mobile element insertion2nstd211human GRCh38 chr12: 111,404,194-111,404,194 , GRCh37.p13 chr12: 111,841,998-111,841,998 SH2B3
    nsv5513157copy number variation1nstd206human GRCh38 chr12: 111,415,249-111,415,495 , GRCh37.p13 chr12: 111,853,053-111,853,299 SH2B3
    nsv5512398copy number variation1nstd206human GRCh38 chr12: 111,416,149-111,421,448 , GRCh37.p13 chr12: 111,853,953-111,859,252 SH2B3
    nsv5433426mobile element insertion1nstd206human GRCh38 chr12: 111,404,194-111,404,245 , GRCh37.p13 chr12: 111,841,998-111,842,049 SH2B3
    nsv5139671mobile element insertion1nstd203human GRCh38 chr12: 111,404,184-111,404,194 , GRCh37.p13 chr12: 111,841,988-111,841,998 SH2B3
    nsv5122352mobile element insertion1nstd203human GRCh38 chr12: 111,404,179-111,404,194 , GRCh37.p13 chr12: 111,841,983-111,841,998 SH2B3
    nsv4995625copy number variation1nstd200human GRCh38 chr12: 111,433,832-111,439,476 , GRCh37.p13 chr12: 111,871,636-111,877,280 SH2B3
    nsv4995624copy number variation1nstd200human GRCh38 chr12: 111,430,026-111,437,342 , GRCh37.p13 chr12: 111,867,830-111,875,146 SH2B3
    nsv4995623copy number variation1nstd200human GRCh38 chr12: 111,422,688-111,429,408 , GRCh37.p13 chr12: 111,860,492-111,867,212 SH2B3
    nsv4993681copy number variation1nstd200human GRCh38 chr12: 111,418,848-111,419,406 , GRCh37.p13 chr12: 111,856,652-111,857,210 SH2B3
    nsv4848761copy number variation1nstd200human GRCh37 chr12: 111,871,636-111,877,280 , GRCh38.p12 chr12: 111,433,832-111,439,476 SH2B3
    nsv4838461copy number variation1nstd200human GRCh37 chr12: 111,860,492-111,867,217 , GRCh38.p12 chr12: 111,422,688-111,429,413 SH2B3
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
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