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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054117inversion1nstd229human GRCh38 chr2: 162,194,703-162,194,788 , GRCh37.p13 chr2: 163,051,213-163,051,298 FAP
    nsv7050848inversion1nstd229human GRCh38 chr2: 162,229,815-162,307,025 , GRCh37.p13 chr2: 163,086,325-163,163,535 FAP, LOC105373724, 1 more genes
    nsv7050735inversion1nstd229human GRCh38 chr2: 162,239,955-162,246,679 , GRCh37.p13 chr2: 163,096,465-163,103,189 FAP, LOC105373724
    nsv7041761inversion1nstd229human GRCh38 chr2: 161,208,254-165,696,625 , GRCh37.p13 chr2: 162,064,765-166,553,135 SCN3A, LOC101929532, 45 more genes
    nsv7041527inversion1nstd229human GRCh38 chr2: 162,239,961-162,244,146 , GRCh37.p13 chr2: 163,096,471-163,100,656 LOC105373724, FAP
    nsv7039552inversion1nstd229human GRCh38 chr2: 161,275,467-165,696,611 , GRCh37.p13 chr2: 162,131,978-166,553,121 LOC105373722, EIF3EP3, 42 more genes
    nsv6697650copy number variation1nstd229human GRCh38 chr2: 162,215,507-162,217,071 , GRCh37.p13 chr2: 163,072,017-163,073,581 FAP
    nsv6690721copy number variation1nstd229human GRCh38 chr2: 162,182,101-162,183,800 , GRCh37.p13 chr2: 163,038,611-163,040,310 FAP
    nsv6355212copy number variation1nstd223human GRCh38 chr2: 162,215,507-162,217,071 , GRCh37.p13 chr2: 163,072,017-163,073,581 FAP
    nsv6346195copy number variation1nstd223human GRCh38 chr2: 162,218,101-162,219,500 , GRCh37.p13 chr2: 163,074,611-163,076,010 FAP
    nsv6344887copy number variation1nstd223human GRCh38 chr2: 162,240,402-162,241,043 , GRCh37.p13 chr2: 163,096,912-163,097,553 FAP
    nsv6343601copy number variation1nstd223human GRCh38 chr2: 162,233,501-162,238,200 , GRCh37.p13 chr2: 163,090,011-163,094,710 FAP
    nsv6337578copy number variation1nstd223human GRCh38 chr2: 162,208,701-162,210,300 , GRCh37.p13 chr2: 163,065,211-163,066,810 FAP
    nsv6336563copy number variation1nstd223human GRCh38 chr2: 162,190,956-162,191,510 , GRCh37.p13 chr2: 163,047,466-163,048,020 FAP
    nsv6335936copy number variation1nstd223human GRCh38 chr2: 162,171,401-162,174,100 , GRCh37.p13 chr2: 163,027,911-163,030,610 FAP, LOC101929532
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315160copy number variation1nstd102humanPathogenic GRCh37 chr2: 160,347,642-174,075,851 , GRCh38.p12 chr2: 159,491,131-173,211,123 EIF3EP3, FAP, 158 more genes
    nsv6313780copy number variation1nstd102humanPathogenic GRCh37 chr2: 161,551,326-167,762,790 , GRCh38.p12 chr2: 160,694,815-166,906,280 SCN9A, FIGN, 60 more genes
    nsv6313568copy number variation1nstd102humanPathogenic GRCh37 chr2: 158,950,827-164,456,735 , GRCh38.p12 chr2: 158,094,315-163,600,225 PSMD14-DT, DPP4, 70 more genes
    nsv6134511copy number variation1nstd213human GRCh37 chr2: 162,990,000-163,060,001 , GRCh38.p12 chr2: 162,133,490-162,203,491 FAP, GCG, 1 more genes
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