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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5884556copy number variation1nstd209human GRCh38 chr1: 179,104,544-179,104,593 , GRCh37.p13 chr1: 179,073,679-179,073,728 ABL2
    nsv5876523copy number variation1nstd209human GRCh38 chr1: 179,095,258-179,097,563 , GRCh37.p13 chr1: 179,064,393-179,066,698 ABL2, TOR3A
    nsv5828757copy number variation1nstd209human GRCh38 chr1: 179,196,742-179,201,159 , GRCh37.p13 chr1: 179,165,877-179,170,294 ABL2, EIF4A1P11
    nsv5828563copy number variation1nstd209human GRCh38 chr1: 179,095,146-179,097,645 , GRCh37.p13 chr1: 179,064,281-179,066,780 ABL2, TOR3A
    nsv5684361mobile element insertion1nstd211human GRCh38 chr1: 179,157,955-179,157,955 , GRCh37.p13 chr1: 179,127,090-179,127,090 ABL2
    nsv5433895copy number variation1nstd206human GRCh38 chr1: 179,140,851-179,140,914 , GRCh37.p13 chr1: 179,109,986-179,110,049 ABL2
    nsv5430538copy number variation1nstd206human GRCh38 chr1: 179,196,000-179,201,000 , GRCh37.p13 chr1: 179,165,135-179,170,135 EIF4A1P11, ABL2
    nsv5427750copy number variation1nstd206human GRCh38 chr1: 179,229,734-179,229,811 , GRCh37.p13 chr1: 179,198,869-179,198,946 ABL2
    nsv5425744copy number variation1nstd206human GRCh38 chr1: 179,196,000-179,201,200 , GRCh37.p13 chr1: 179,165,135-179,170,335 EIF4A1P11, ABL2
    nsv5425541copy number variation1nstd206human GRCh38 chr1: 179,227,888-179,228,219 , GRCh37.p13 chr1: 179,197,023-179,197,354 ABL2
    nsv5423300copy number variation1nstd206human GRCh38 chr1: 179,210,707-179,217,525 , GRCh37.p13 chr1: 179,179,842-179,186,660 ABL2
    nsv5417447copy number variation1nstd206human GRCh38 chr1: 179,095,261-179,097,564 , GRCh37.p13 chr1: 179,064,396-179,066,699 ABL2, TOR3A
    nsv5411258mobile element insertion1nstd206human GRCh38 chr1: 179,157,955-179,158,006 , GRCh37.p13 chr1: 179,127,090-179,127,141 ABL2
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5347336translocation1nstd200human GRCh38 chr1: 179,216,111-179,216,111 , GRCh38 chr1: 179,216,028-179,216,028 , GRCh37.p13 chr1: 179,185,163-179,185,163 , GRCh37.p13 chr1: 179,185,246-179,185,246 ABL2
    nsv5347335translocation1nstd200human GRCh38 chr1: 179,097,564-179,097,564 , GRCh38 chr1: 179,095,261-179,095,261 , GRCh37.p13 chr1: 179,066,699-179,066,699 , GRCh37.p13 chr1: 179,064,396-179,064,396 TOR3A, ABL2
    nsv5286967copy number variation1nstd204human GRCh38.p13 chr1: 179,195,945-179,201,480 , GRCh37.p13 chr1: 179,165,080-179,170,615 ABL2, EIF4A1P11
    nsv5219047copy number variation1nstd204human GRCh38.p13 chr1: 179,195,801-179,198,500 , GRCh37.p13 chr1: 179,164,936-179,167,635 ABL2
    nsv5215883copy number variation1nstd204human GRCh38.p13 chr1: 179,195,501-179,197,528 , GRCh37.p13 chr1: 179,164,636-179,166,663 ABL2
    nsv5215293copy number variation1nstd204human GRCh38.p13 chr1: 179,195,651-179,202,936 , GRCh37.p13 chr1: 179,164,786-179,172,071 EIF4A1P11, ABL2
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