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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5897454copy number variation1nstd209human GRCh38 chr2: 201,221,824-201,490,725 , GRCh37.p13 chr2: 202,086,547-202,355,448 CASP8, CASP10, 5 more genes
    nsv5564426copy number variation1nstd102humanUncertain significance GRCh37 chr2: 202,334,676-202,523,241 , GRCh38.p12 chr2: 201,469,953-201,658,518 MTCO1P16, MTND3P16, 11 more genes
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5434451copy number variation1nstd206human GRCh38 chr2: 201,449,296-201,453,100 , GRCh37.p13 chr2: 202,314,019-202,317,823 STRADB, TRAK2
    nsv5318436copy number variation1nstd204human GRCh37.p13 chr2: 202,325,351-202,356,117 , GRCh38.p13 chr2: 201,460,628-201,491,394 C2CD6, STRADB
    nsv5211947copy number variation1nstd204human GRCh38.p13 chr2: 201,460,601-201,491,400 , GRCh37.p13 chr2: 202,325,324-202,356,123 C2CD6, STRADB
    nsv5204712copy number variation1nstd204human GRCh38.p13 chr2: 201,460,715-201,472,407 , GRCh37.p13 chr2: 202,325,438-202,337,130 STRADB
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4728199copy number variation1nstd102humanUncertain significance GRCh37 chr2: 202,011,822-202,749,788 , GRCh38.p12 chr2: 201,147,099-201,885,065 MTCO1P16, CFLAR, 26 more genes
    nsv4728174copy number variation1nstd102humanUncertain significance GRCh37 chr2: 202,333,474-202,450,459 , GRCh38.p12 chr2: 201,468,751-201,585,736 MTCO2P16, STRADB, 7 more genes
    nsv4674609copy number variation1nstd102humanUncertain significance GRCh37 chr2: 202,333,474-202,537,984 , GRCh38.p12 chr2: 201,468,751-201,673,261 C2CD6, MTCO1P16, 11 more genes
    nsv4674597copy number variation1nstd102humanPathogenic GRCh37 chr2: 201,106,432-204,901,548 , GRCh38.p12 chr2: 200,241,709-204,036,825 KIAA2012-AS1, SNORD11, 113 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 SNORA41, LOC101929633, 663 more genes
    nsv4465222mobile element insertion1nstd166human GRCh37.p13 chr2: 202,345,975-202,345,975 , GRCh38.p12 chr2: 201,481,252-201,481,252 STRADB
    nsv4436532copy number variation1nstd102humanPathogenic GRCh37 chr2: 188,926,928-225,298,653 , GRCh38.p12 chr2: 188,062,201-224,433,936 MARS2, KRT18P19, 575 more genes
    nsv4316119inversion1nstd166human GRCh37.p13 chr2: 187,130,612-218,396,189 , GRCh38.p12 chr2: 186,265,885-217,531,466 , ACADL, 453 more genes
    nsv3924199copy number variation1nstd102humanUncertain significance NCBI36 chr2: 130,861,065-242,751,149 , GRCh37.p13 chr2: 131,144,595-243,102,476 , GRCh38.p12 chr2: 130,387,022-242,160,331 METAP1D, UBE2E3-DT, 1635 more genes
    nsv3923963copy number variation1nstd102humanUncertain significance NCBI36 chr2: 110,190,938-242,751,149 , GRCh37.p13 chr2: 110,833,649-243,102,476 , GRCh38.p12 chr2: 110,076,072-242,160,331 NMTRQ-TTG9-1, MIR6810, 1944 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3908231copy number variation1nstd102humanPathogenic NCBI36 chr2: 196,233,563-204,542,456 , GRCh38 chr2: 195,660,594-203,969,488 , GRCh37 chr2: 196,525,318-204,834,211 LINC01877, MAIP1, 170 more genes
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