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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4674643copy number variation1nstd102humanUncertain significance GRCh37 chr2: 180,557,719-180,850,879 , GRCh38.p12 chr2: 179,692,992-179,986,152 CWC22, TXNL4AP1, 2 more genes
    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 CWC22, 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 CWC22, TRE-TTC9-1, 412 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 CWC22, LINC01877, 326 more genes
    nsv4451512copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,329,586-192,756,373 , GRCh38.p12 chr2: 166,473,076-191,891,647 CWC22, LINC01117, 339 more genes
    nsv4674757copy number variation1nstd102humanPathogenic GRCh37 chr2: 174,690,039-195,521,582 , GRCh38.p12 chr2: 173,825,311-194,656,858 CWC22, 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 CWC22, CALCRL-AS1, 218 more genes
    nsv3878976copy number variation1nstd102humanPathogenic GRCh37 chr2: 177,315,153-196,375,520 , GRCh38.p12 chr2: 176,450,425-195,510,796 CWC22, FSIP2-AS1, 202 more genes
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 CWC22, RBM45, 258 more genes
    nsv3904056copy number variation1nstd102humanPathogenic GRCh37 chr2: 164,821,892-183,059,789 , NCBI36 chr2: 164,530,138-182,768,034 , GRCh38 chr2: 163,965,382-182,195,062 CWC22, PRKRA, 256 more genes
    nsv3891673copy number variation1nstd102humanPathogenic GRCh37 chr2: 172,285,743-190,044,294 , GRCh38 chr2: 171,429,233-189,179,568 , NCBI36 chr2: 171,993,989-189,752,539 CWC22, LOC729141, 238 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 CWC22, 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 CWC22, RPL23AP35, 211 more genes
    nsv3894385copy number variation1nstd102humanPathogenic NCBI36 chr2: 170,972,444-186,762,866 , GRCh37 chr2: 171,264,198-187,054,621 , GRCh38 chr2: 170,407,688-186,189,894 CWC22, KRT18P29, 220 more genes
    nsv3892770copy number variation1nstd102humanPathogenic GRCh37 chr2: 175,499,230-189,865,690 , GRCh38 chr2: 174,634,502-189,000,964 , NCBI36 chr2: 175,207,476-189,573,935 CWC22, LOC401021, 179 more genes
    nsv4454648copy number variation1nstd102humanPathogenic GRCh37 chr2: 173,538,954-186,401,606 , GRCh38.p12 chr2: 172,674,226-185,536,879 CWC22, PDE11A, 176 more genes
    nsv5381341copy number variation1nstd102humanPathogenic GRCh37 chr2: 171,999,572-182,774,361 , GRCh38.p12 chr2: 171,143,062-181,909,634 CWC22, ALDH7A1P2, 174 more genes
    nsv3888432copy number variation1nstd102humanPathogenic GRCh37 chr2: 174,238,257-181,604,341 , GRCh38.p12 chr2: 173,373,529-180,739,614 CWC22, LRRC2P1, 125 more genes
    nsv3920257copy number variation1nstd102humanPathogenic NCBI36 chr2: 173,710,846-180,977,641 , GRCh37.p13 chr2: 174,002,600-181,269,396 , GRCh38.p12 chr2: 173,137,872-180,404,669 CWC22, LINC01117, 128 more genes
    nsv3900249copy number variation1nstd102humanPathogenic NCBI36 chr2: 174,809,425-181,761,818 , GRCh38 chr2: 174,236,451-181,188,846 , GRCh37 chr2: 175,101,179-182,053,573 CWC22, EXTL2P1, 120 more genes
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