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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6696987copy number variation1nstd229human GRCh38 chr2: 151,204,847-151,461,229 , GRCh37.p13 chr2: 152,061,361-152,317,743 LOC107985827, MIR4773-1, 7 more genes
    nsv6696411copy number variation1nstd229human GRCh38 chr2: 151,299,686-151,544,761 , GRCh37.p13 chr2: 152,156,200-152,401,275 TNFAIP6, RN7SL124P, 6 more genes
    nsv6693184copy number variation1nstd229human GRCh38 chr2: 151,256,866-151,538,730 , GRCh37.p13 chr2: 152,113,380-152,395,244 NEB, NMI, 8 more genes
    nsv6692524copy number variation1nstd229human GRCh38 chr2: 150,229,231-153,083,013 , GRCh37.p13 chr2: 151,085,745-153,939,527 RPL30P2, NEB, 30 more genes
    nsv6689852copy number variation1nstd229human GRCh38 chr2: 150,910,105-152,531,708 , GRCh37.p13 chr2: 151,766,619-153,388,222 NUDCP1, FABP5P10, 19 more genes
    nsv6678548copy number variation1nstd229human GRCh38 chr2: 151,280,855-151,620,736 , GRCh37.p13 chr2: 152,137,369-152,477,250 RIF1, LOC107985827, 7 more genes
    nsv6627351copy number variation1nstd224human GRCh37 chr2: 152,210,713-152,236,398 , GRCh38.p12 chr2: 151,354,199-151,379,884 MIR4773-2, TNFAIP6, 3 more genes
    nsv6541714inversion1nstd223human GRCh38 chr2: 148,865,353-155,671,569 , GRCh37.p13 chr2: 149,622,922-156,528,081 , LOC107985952, 79 more genes
    nsv6351407copy number variation1nstd223human GRCh38 chr2: 151,256,866-151,538,730 , GRCh37.p13 chr2: 152,113,380-152,395,244 TNFAIP6, NMI, 8 more genes
    nsv6345825copy number variation1nstd223human GRCh38 chr2: 151,200,703-151,458,677 , GRCh37.p13 chr2: 152,057,217-152,315,191 MIR4773-2, NMI, 7 more genes
    nsv6342704copy number variation1nstd223human GRCh38 chr2: 151,160,100-151,450,583 , GRCh37.p13 chr2: 152,016,614-152,307,097 RIF1, MIR4773-1, 9 more genes
    nsv6335612copy number variation1nstd223human GRCh38 chr2: 151,280,855-151,620,736 , GRCh37.p13 chr2: 152,137,369-152,477,250 NEB, MIR4773-1, 7 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313481copy number variation1nstd102humanPathogenic GRCh37 chr2: 143,258,712-152,867,819 , GRCh38.p12 chr2: 142,501,143-152,011,305 STIP1P1, RNU6-715P, 98 more genes
    nsv6290982copy number variation1nstd102humanPathogenic GRCh37 chr2: 142,409,401-152,680,804 , GRCh38.p12 chr2: 141,651,832-151,824,290 LOC101928526, MTCO2P5, 101 more genes
    nsv6134503copy number variation1nstd213human GRCh37 chr2: 152,210,000-152,310,001 , GRCh38.p12 chr2: 151,353,486-151,453,487 TNFAIP6, RIF1, 4 more genes
    nsv6134500copy number variation1nstd213human GRCh37 chr2: 149,790,000-179,310,001 , GRCh38.p12 chr2: 148,934,069-178,445,274 , ACVR1, 394 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
    nsv5444636copy number variation1nstd206human GRCh38 chr2: 150,863,589-152,862,185 , GRCh37.p13 chr2: 151,720,103-153,718,699 , CACNB4, 24 more genes
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