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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 MYO1B, DAZAP2P1, 2991 more genes
    nsv3894939copy number variation1nstd102humanPathogenic NCBI36 chr2: 175,471,822-204,514,516 , GRCh37 chr2: 175,763,576-204,806,271 , GRCh38 chr2: 174,898,848-203,941,548 MYO1B, TRE-TTC9-1, 412 more genes
    nsv6315398copy number variation1nstd102humanPathogenic GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349 MYO1B, LOC107985785, 381 more genes
    nsv3899404copy number variation1nstd102humanPathogenic NCBI36 chr2: 176,877,419-202,612,758 , GRCh37 chr2: 177,169,173-202,904,513 , GRCh38 chr2: 176,304,445-202,039,790 MYO1B, LINC01877, 326 more genes
    nsv4451512copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,329,586-192,756,373 , GRCh38.p12 chr2: 166,473,076-191,891,647 MYO1B, LINC01117, 339 more genes
    nsv4674757copy number variation1nstd102humanPathogenic GRCh37 chr2: 174,690,039-195,521,582 , GRCh38.p12 chr2: 173,825,311-194,656,858 MYO1B, OSBPL6, 256 more genes
    nsv3895293copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,738,797-199,390,216 , NCBI36 chr2: 178,447,043-199,098,461 , GRCh38 chr2: 177,874,070-198,525,492 MYO1B, CALCRL-AS1, 218 more genes
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 MYO1B, LOC100421409, 310 more genes
    nsv3878976copy number variation1nstd102humanPathogenic GRCh37 chr2: 177,315,153-196,375,520 , GRCh38.p12 chr2: 176,450,425-195,510,796 MYO1B, FSIP2-AS1, 202 more genes
    nsv3900193copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,692,457-195,990,053 , NCBI36 chr2: 178,400,703-195,698,298 , GRCh38 chr2: 177,827,730-195,125,329 MYO1B, OSBPL6, 171 more genes
    nsv3905582copy number variation1nstd102humanPathogenic GRCh38 chr2: 176,086,763-193,201,970 , NCBI36 chr2: 176,659,737-193,774,941 , GRCh37 chr2: 176,951,491-194,066,696 MYO1B, RPL23AP35, 211 more genes
    nsv3891560copy number variation1nstd102humanPathogenic GRCh38 chr2: 186,027,472-201,059,372 , NCBI36 chr2: 186,600,444-201,632,340 , GRCh37 chr2: 186,892,199-201,924,095 MYO1B, AOX1, 174 more genes
    nsv6636571copy number variation1nstd102humanPathogenic GRCh37 chr2: 187,152,754-199,960,525 , GRCh38.p12 chr2: 186,288,027-199,095,802 MYO1B, GAPDHP59, 135 more genes
    nsv3884561copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,490,490-200,615,496 , GRCh38.p12 chr2: 188,625,763-199,750,773 MYO1B, C2orf88, 120 more genes
    nsv3884912copy number variation1nstd102humanPathogenic GRCh37 chr2: 191,750,202-202,297,376 , GRCh38.p12 chr2: 190,885,476-201,432,653 MYO1B, CLK1, 134 more genes
    nsv3898686copy number variation1nstd102humanPathogenic GRCh37 chr2: 182,623,428-192,880,118 , GRCh38 chr2: 181,758,701-192,015,392 , NCBI36 chr2: 182,331,673-192,588,363 MYO1B, KRT18P19, 111 more genes
    nsv4716529copy number variation1nstd102humanPathogenic GRCh37 chr2: 190,345,272-200,212,289 , GRCh38.p12 chr2: 189,480,546-199,347,566 MYO1B, C2orf66, 105 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 MYO1B, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 MYO1B, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 MYO1B, RNU6-674P, 3735 more genes
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