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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6834393copy number variation1nstd229human GRCh38 chr7: 38,944,248-39,960,814 , GRCh37.p13 chr7: 38,983,848-40,000,413 LOC100422519, LOC646999, 21 more genes
    nsv6827959copy number variation1nstd229human GRCh38 chr7: 39,384,078-39,613,245 , GRCh37.p13 chr7: 39,423,677-39,652,844 POU6F2, LOC105375237, 6 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631946copy number variation1nstd224human GRCh37 chr7: 39,240,060-39,472,874 , GRCh38.p12 chr7: 39,200,461-39,433,275 POU6F2-AS1, POU6F2, 3 more genes
    nsv6609418copy number variation1nstd223human GRCh38 chr7: 39,384,078-39,613,241 , GRCh37.p13 chr7: 39,423,677-39,652,840 LOC646999, POU6F2-AS1, 6 more genes
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313828copy number variation1nstd102humanUncertain significance GRCh37 chr7: 38,883,386-39,488,125 , GRCh38.p12 chr7: 38,843,786-39,448,526 VPS41, POU6F2-AS2, 5 more genes
    nsv6290884copy number variation1nstd102humanUncertain significance GRCh37 chr7: 38,728,844-40,069,964 , GRCh38.p12 chr7: 38,689,244-40,030,365 RALA, POU6F2-AS2, 22 more genes
    nsv6136995copy number variation1nstd213human GRCh37 chr7: 39,040,000-48,190,001 , GRCh38.p12 chr7: 39,000,400-48,150,404 ADCY1, AEBP1, 161 more genes
    nsv6135992copy number variation1nstd213human GRCh37 chr7: 39,290,000-48,200,001 , GRCh38.p12 chr7: 39,250,401-48,160,404 PSMA2, RALA, 160 more genes
    nsv6135763copy number variation1nstd213human GRCh37 chr7: 38,660,000-39,700,001 , GRCh38.p12 chr7: 38,620,400-39,660,402 AMPH, KRT8P20, 15 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4953599copy number variation1nstd200human GRCh38 chr7: 39,393,026-39,442,354 , GRCh37.p13 chr7: 39,432,625-39,481,953 LOC105375238, POU6F2, 1 more genes
    nsv4675334copy number variation1nstd102humanUncertain significance GRCh37 chr7: 38,895,125-39,488,125 , GRCh38.p12 chr7: 38,855,525-39,448,526 VPS41, POU6F2-AS2, 5 more genes
    nsv4675078copy number variation1nstd102humanUncertain significance GRCh37 chr7: 37,202,606-39,500,521 , GRCh38.p12 chr7: 37,163,001-39,460,922 TRGV11, SFRP4, 45 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv3924742copy number variation1nstd102humanPathogenic GRCh37 chr7: 38,217,601-45,343,699 , GRCh38 chr7: 38,177,999-45,304,100 , NCBI36 chr7: 38,184,126-45,310,224 NUDCD3, KRT8P20, 152 more genes
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