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Items: 1 to 20 of 23

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3871100copy number variation1nstd102humanLikely benign GRCh37 chr1: 45,819,488-45,945,384 , GRCh38.p12 chr1: 45,353,816-45,479,712 TESK2, PPIAP36
    nsv4682365copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr1: 45,805,881-45,809,328 , GRCh38.p12 chr1: 45,340,209-45,343,656 TESK2, TOE1, 1 more genes
    nsv4682150copy number variation1nstd102humanUncertain significance GRCh37 chr1: 45,794,978-45,809,328 , GRCh38.p12 chr1: 45,329,306-45,343,656 TESK2, MUTYH, 1 more genes
    nsv7095620copy number variation1nstd102humanUncertain significance GRCh37 chr1: 45,800,053-45,809,328 , GRCh38.p12 chr1: 45,334,381-45,343,656 TESK2, TOE1, 1 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 TESK2, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 TESK2, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 TESK2, RNU1-153P, 4887 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 TESK2, LOC107984940, 407 more genes
    nsv3888489copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 45,303,358-52,157,856 , GRCh38.p12 chr1: 44,837,686-51,692,184 TESK2, CDKN2C, 141 more genes
    nsv3905377copy number variation1nstd102humanLikely benign GRCh37 chr1: 45,935,520-46,686,477 , GRCh38 chr1: 45,469,848-46,220,805 , NCBI36 chr1: 45,708,107-46,459,064 TESK2, MMACHC, 23 more genes
    nsv3879331copy number variation1nstd102humanBenign GRCh37 chr1: 45,819,489-46,245,645 , GRCh38.p12 chr1: 45,353,817-45,779,973 TESK2, RPL7AP16, 14 more genes
    nsv3889126copy number variation1nstd102humanUncertain significance GRCh37 chr1: 45,905,995-46,031,595 , GRCh38.p12 chr1: 45,440,323-45,565,923 TESK2, AKR1A1, 4 more genes
    nsv4674088copy number variation1nstd102humanUncertain significance GRCh37 chr1: 45,386,263-45,982,314 , GRCh38.p12 chr1: 44,920,591-45,516,642 TESK2, TOE1, 17 more genes
    nsv3896519copy number variation1nstd102humanUncertain significance NCBI36 chr1: 45,641,130-45,841,607 , GRCh37 chr1: 45,868,543-46,069,020 , GRCh38 chr1: 45,402,871-45,603,348 TESK2, CCDC163, 6 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 TESK2, LINC01776, 1853 more genes
    nsv3878135copy number variation1nstd102humanUncertain significance GRCh37 chr1: 33,241,563-46,663,513 , GRCh38.p12 chr1: 32,775,962-46,197,841 TESK2, LINC02786, 365 more genes
    nsv7095531copy number variation1nstd102humanUncertain significance GRCh37 chr1: 44,257,753-46,663,493 , GRCh38.p12 chr1: 43,792,082-46,197,821 TESK2, AKR1A1, 87 more genes
    nsv6314936copy number variation1nstd102humanUncertain significance GRCh37 chr1: 44,346,001-46,332,161 , GRCh38.p12 chr1: 43,880,329-45,866,489 TESK2, ZSWIM5, 79 more genes
    nsv3881136copy number variation1nstd102humanUncertain significance GRCh37 chr1: 45,715,667-46,501,705 , GRCh38.p12 chr1: 45,249,995-46,036,033 TESK2, AKR1A1, 22 more genes
    nsv3902893copy number variation1nstd102humanUncertain significance GRCh38 chr1: 45,488,251-46,220,805 , NCBI36 chr1: 45,726,510-46,459,064 , GRCh37 chr1: 45,953,923-46,686,477 TESK2, CCDC163, 23 more genes
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