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Items: 1 to 20 of 158

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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
    nsv5450895copy number variation1nstd206human GRCh38 chr2: 141,459,078-156,842,302 , GRCh37.p13 chr2: 142,216,647-157,698,814 , LOC105373696, 163 more genes
    nsv5450173copy number variation1nstd206human GRCh38 chr2: 152,810,169-152,941,544 , GRCh37.p13 chr2: 153,666,683-153,798,058 UBQLN4P2
    nsv5448351copy number variation1nstd206human GRCh38 chr2: 151,571,812-153,829,571 , GRCh37.p13 chr2: 152,428,326-154,686,084 , LOC105373691, 20 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
    nsv5283186copy number variation1nstd204human GRCh38.p13 chr2: 152,860,469-152,909,349 , GRCh37.p13 chr2: 153,716,983-153,765,863 UBQLN4P2
    nsv5208271copy number variation1nstd204human GRCh38.p13 chr2: 152,860,399-152,879,852 , GRCh37.p13 chr2: 153,716,913-153,736,366 UBQLN4P2
    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
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4674226copy number variation1nstd102humanPathogenic GRCh37 chr2: 147,173,792-158,346,266 , GRCh38.p12 chr2: 146,416,224-157,489,754 RBM43, LINC01931, 120 more genes
    nsv4582602copy number variation1nstd183human GRCh37 chr2: 153,666,770-153,798,065 , GRCh38.p12 chr2: 152,810,256-152,941,551 UBQLN4P2
    nsv4406268copy number variation1nstd174human GRCh37 chr2: 153,666,725-153,798,065 , GRCh38.p12 chr2: 152,810,211-152,941,551 UBQLN4P2
    nsv4088338copy number variation1nstd166human GRCh37.p13 chr2: 153,716,993-153,765,861 , GRCh38.p12 chr2: 152,860,479-152,909,347 UBQLN4P2
    nsv4081790copy number variation1nstd166human GRCh37.p13 chr2: 153,666,699-153,798,009 , GRCh38.p12 chr2: 152,810,185-152,941,495 UBQLN4P2
    nsv4076454copy number variation1nstd166human GRCh37.p13 chr2: 153,625,850-153,860,681 , GRCh38.p12 chr2: 152,769,336-153,004,167 LOC105373691, UBQLN4P2
    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
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