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Items: 1 to 20 of 11593

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131356insertion1nstd186human GRCh37 chr14: 106,201,876-106,201,876 , GRCh38.p12 chr14|NT_187600.1: 203,308-203,308 , GRCh38.p12 chr14: 105,735,539-105,735,539 IGH
    nsv6130987insertion1nstd186human GRCh37 chr14: 106,212,784-106,212,784 , GRCh38.p12 chr14|NT_187600.1: 214,216-214,216 , GRCh38.p12 chr14: 105,746,447-105,746,447 IGH
    nsv6130764insertion1nstd186human GRCh37 chr14: 106,188,923-106,188,962 , GRCh38.p12 chr14: 105,722,586-105,722,625 , GRCh38.p12 chr14|NT_187600.1: 190,355-190,394 IGH, IGHEP1
    nsv6130744insertion1nstd186human GRCh37 chr14: 106,873,737-106,873,737 , GRCh38.p12 chr14: 106,417,820-106,417,820 , GRCh38.p12 chr14|NT_187600.1: 909,499-909,499 IGH, IGHVIII-38-1
    nsv6129237insertion1nstd186human GRCh37 chr14: 106,874,356-106,874,356 , GRCh38.p12 chr14: 106,418,439-106,418,439 , GRCh38.p12 chr14|NT_187600.1: 910,118-910,118 IGH, IGHVIII-38-1
    nsv6121671copy number variation1nstd186human GRCh37 chr14: 106,789,206-106,790,042 , GRCh38.p12 chr14: 106,333,284-106,334,119 , GRCh38.p12 chr14|NT_187600.1: 801,053-801,888 IGH, IGHV3-30, 1 more genes
    nsv6121205copy number variation1nstd186human GRCh37 chr14: 106,162,749-106,162,819 , GRCh38.p12 chr14|NT_187600.1: 164,181-164,251 , GRCh38.p12 chr14: 105,696,412-105,696,482 IGH
    nsv6113763copy number variation1nstd186human GRCh37 chr14: 106,866,550-106,876,051 , GRCh38.p12 chr14: 106,410,637-106,420,137 , GRCh38.p12 chr14|NT_187600.1: 902,316-911,816 IGH, IGHVIII-38-1, 2 more genes
    nsv6112828copy number variation1nstd186human GRCh37 chr14: 106,071,380-106,178,036 , GRCh38.p12 chr14|NT_187600.1: 72,812-179,468 , GRCh38.p12 chr14: 105,605,043-105,711,699 , ELK2AP, 9 more genes
    nsv5393654mobile element deletion1nstd186human GRCh37 chr14: 106,723,481-106,723,835 , GRCh38.p12 chr14|NT_187600.1: 734,657-735,011 , GRCh38.p12 chr14: 106,266,888-106,267,242 IGHV3-23, IGH
    nsv5393394copy number variation1nstd186human GRCh37 chr14: 106,330,469-106,471,244 , GRCh38.p12 chr14: 105,864,259-106,005,095 , GRCh38.p12 chr14|NT_187600.1: 332,028-472,864 RPS8P1, IGHD3-16, 42 more genes
    nsv5393317copy number variation1nstd186human GRCh37 chr14: 106,330,468-106,361,495 , GRCh38.p12 chr14: 105,864,258-105,895,637 , GRCh38.p12 chr14|NT_187600.1: 332,027-363,406 IGHJ3, IGHD2-21, 18 more genes
    nsv5393311copy number variation1nstd186human GRCh37 chr14: 106,094,235-106,094,691 , GRCh38.p12 chr14|NT_187600.1: 95,667-96,123 , GRCh38.p12 chr14: 105,627,898-105,628,354 IGH
    nsv5393259copy number variation1nstd186human GRCh37 chr14: 106,212,042-106,326,104 , GRCh38.p12 chr14: 105,786,368-105,859,884 , GRCh38.p12 chr14|NT_187600.1: 254,137-327,653 IGH, IGHD, 6 more genes
    nsv5393186copy number variation1nstd186human GRCh37 chr14: 106,372,880-106,382,388 , GRCh38.p12 chr14: 105,907,022-105,916,529 , GRCh38.p12 chr14|NT_187600.1: 374,791-384,298 IGH, FAM30A, 7 more genes
    nsv5393174copy number variation1nstd186human GRCh37 chr14: 106,330,466-106,373,070 , GRCh38.p12 chr14: 105,864,256-105,907,212 , GRCh38.p12 chr14|NT_187600.1: 332,025-374,981 IGHJ5, IGHD3-10, 26 more genes
    nsv5393147copy number variation1nstd186human GRCh37 chr14: 106,880,205-106,880,589 , GRCh38.p12 chr14: 106,424,299-106,424,683 , GRCh38.p12 chr14|NT_187600.1: 915,978-916,362 IGH, IGHV7-40
    nsv5393137copy number variation1nstd186human GRCh37 chr14: 106,330,468-106,350,728 , GRCh38.p12 chr14|NT_187600.1: 332,027-352,639 , GRCh38.p12 chr14: 105,864,258-105,884,870 IGHJ4, IGHJ2P, 12 more genes
    nsv5393073copy number variation1nstd186human GRCh37 chr14: 106,330,467-107,034,727 , GRCh38.p12 chr14: 105,864,257-106,578,742 , GRCh38.p12 chr14|NT_187600.1: 420,111-1,214,078 , IGHV3-60, 159 more genes
    nsv5392952copy number variation1nstd186human GRCh37 chr14: 106,373,076-106,382,392 , GRCh38.p12 chr14: 105,907,218-105,916,533 , GRCh38.p12 chr14|NT_187600.1: 374,987-384,302 IGH, FAM30A, 7 more genes
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