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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056410inversion1nstd229human GRCh38 chr2: 155,671,571-160,808,437 , GRCh37.p13 chr2: 156,528,083-161,664,948 LOC105373714, PKP4-AS1, 64 more genes
    nsv7050082inversion1nstd229human GRCh38 chr2: 154,880,025-156,722,310 , GRCh37.p13 chr2: 155,736,537-157,578,822 LOC105373703, LOC107985828, 25 more genes
    nsv7048490inversion1nstd229human GRCh38 chr2: 156,054,444-158,055,095 , GRCh37.p13 chr2: 156,910,956-158,911,607 CYTIP, LINC01876, 23 more genes
    nsv7038090inversion1nstd229human GRCh38 chr2: 152,079,952-160,943,714 , GRCh37.p13 chr2: 152,936,466-161,800,225 , ITGB6, 105 more genes
    nsv6683078copy number variation1nstd229human GRCh38 chr2: 154,503,385-158,170,825 , GRCh37.p13 chr2: 155,359,897-159,027,337 HEBP2P1, RNU6-436P, 48 more genes
    nsv6636792copy number variation1nstd102humanUncertain significance GRCh37 chr2: 156,528,912-158,233,672 , GRCh38.p12 chr2: 155,672,400-157,377,160 RN7SKP281, HEBP2P1, 17 more genes
    nsv6636385copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr2: 156,139,856-156,515,520 , GRCh37 chr2: 156,996,368-157,372,032 GPD2, NR4A2, 4 more genes
    nsv6545135inversion1nstd223human GRCh38 chr2: 151,746,038-156,373,752 , GRCh37.p13 chr2: 152,602,552-157,230,264 , PRPF40A, 46 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6291446copy number variation1nstd102humanPathogenic GRCh37 chr2: 154,328,530-158,759,642 , GRCh38.p12 chr2: 153,472,016-157,903,130 RNU6-1001P, LOC105373709, 47 more genes
    nsv6291262copy number variation1nstd102humannot provided GRCh37 chr2: 152,967,964-160,089,210 , GRCh38.p12 chr2: 152,111,450-159,232,699 GALNT13-AS1, ARL6IP6, 85 more genes
    nsv6291000copy number variation1nstd102humanPathogenic GRCh37 chr2: 154,852,961-159,126,250 , GRCh38.p12 chr2: 153,996,448-158,269,738 LINC01876, ACVR1C, 52 more genes
    nsv6290940copy number variation1nstd102humanPathogenic GRCh37 chr2: 157,058,119-157,183,736 , GRCh38.p12 chr2: 156,201,607-156,327,224 NR4A2, LINC01876
    nsv6134500copy number variation1nstd213human GRCh37 chr2: 149,790,000-179,310,001 , GRCh38.p12 chr2: 148,934,069-178,445,274 , ACVR1, 394 more genes
    nsv5687480mobile element insertion1nstd211human GRCh38 chr2: 156,330,951-156,330,951 , GRCh37.p13 chr2: 157,187,463-157,187,463 NR4A2
    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
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5404094mobile element insertion1nstd206human GRCh38 chr2: 156,330,951-156,331,002 , GRCh37.p13 chr2: 157,187,463-157,187,514 NR4A2
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