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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5327227inversion1nstd204human GRCh37.p13 chr2: 151,300,232-168,612,803 , GRCh38.p13 chr2: 150,443,718-167,756,293 , RND3, 198 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4916094copy number variation1nstd200human GRCh38 chr2: 162,133,378-162,142,755 , GRCh37.p13 chr2: 162,989,888-162,999,265 GCG, LOC101929532
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4728409copy number variation1nstd102humanUncertain significance GRCh37 chr2: 162,620,633-163,421,321 , GRCh38.p12 chr2: 161,764,123-162,564,811 LOC105373724, EIF3EP2, 13 more genes
    nsv4685668copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 160,075,929-164,666,149 , GRCh38.p12 chr2: 159,219,418-163,809,639 DPP4, FAP, 53 more genes
    nsv4685660copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 161,561,653-163,178,787 , GRCh38.p12 chr2: 160,705,142-162,322,277 DPP4, FAP, 24 more genes
    nsv4463953mobile element insertion1nstd166human GRCh37.p13 chr2: 163,007,684-163,007,684 , GRCh38.p12 chr2: 162,151,174-162,151,174 GCG, LOC101929532
    nsv4346986copy number variation1nstd102humanPathogenic GRCh37 chr2: 162,485,583-168,295,583 , GRCh38.p12 chr2: 161,629,073-167,439,073 CYP2C56P, LOC101929532, 49 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
    nsv3921931copy number variation1nstd102humanPathogenic NCBI36 chr2: 161,464,472-165,033,549 , GRCh37.p13 chr2: 161,756,226-165,325,303 , GRCh38.p12 chr2: 160,899,715-164,468,793 MXRA7P1, LINC01806, 35 more genes
    nsv3921316copy number variation1nstd102humanPathogenic NCBI36 chr2: 155,624,215-165,414,901 , GRCh37.p13 chr2: 155,915,969-165,706,655 , GRCh38.p12 chr2: 155,059,457-164,850,145 LOC105373712, MTCO1P45, 121 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
    nsv3904389copy number variation1nstd102humanPathogenic GRCh38 chr2: 158,382,388-166,605,758 , GRCh37 chr2: 159,238,900-167,462,268 , NCBI36 chr2: 158,947,146-167,170,514 TANC1, SCN1A, 95 more genes
    nsv3902725copy number variation1nstd102humanPathogenic NCBI36 chr2: 154,931,546-167,613,658 , GRCh38 chr2: 154,366,788-167,048,902 , GRCh37 chr2: 155,223,300-167,905,412 SCN2A, LOC102724058, 148 more genes
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