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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096276copy number variation1nstd102humanUncertain significance GRCh37 chr21: 15,554,059-16,340,513 , GRCh38.p12 chr21: 14,181,738-14,968,192 RBM11, LIPI, 11 more genes
    nsv7027840copy number variation1nstd229human GRCh38 chr21: 14,377,890-22,678,900 , GRCh37.p13 chr21: 15,750,211-24,051,220 C1QBPP1, VDAC2P1, 74 more genes
    nsv7026148copy number variation1nstd229human GRCh38 chr21: 14,376,114-14,416,558 , GRCh37.p13 chr21: 15,748,435-15,788,879 LOC105369304, HSPA13
    nsv7024691copy number variation1nstd229human GRCh38 chr21: 14,376,301-14,377,900 , GRCh37.p13 chr21: 15,748,622-15,750,221 HSPA13
    nsv7022640copy number variation1nstd229human GRCh38 chr21: 14,357,098-14,406,346 , GRCh37.p13 chr21: 15,729,419-15,778,667 LOC105369304, HSPA13
    nsv6637761copy number variation1nstd102humanUncertain significance GRCh37 chr21: 15,006,458-21,778,529 , GRCh38.p12 chr21: 13,634,137-20,406,217 ASMER1, ERLEC1P1, 91 more genes
    nsv6637251copy number variation1nstd102humanUncertain significance GRCh37 chr21: 15,023,402-17,685,941 , GRCh38.p12 chr21: 13,651,081-16,313,620 LOC105369292, ABCC13, 51 more genes
    nsv6634469copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-29,046,428 , GRCh38.p12 chr21: 13,634,136-27,674,109 ADAMTS5, VN2R20P, 160 more genes
    nsv6626852copy number variation1nstd224human GRCh37 chr21: 15,248,281-16,213,169 , GRCh38.p12 chr21: 13,875,960-14,840,848 GAPDHP16, ANKRD20A11P, 22 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
    nsv6555000copy number variation1nstd223human GRCh38 chr21: 14,371,662-14,372,255 , GRCh37.p13 chr21: 15,743,983-15,744,576 HSPA13
    nsv6552015copy number variation1nstd223human GRCh38 chr21: 14,371,990-14,372,443 , GRCh37.p13 chr21: 15,744,311-15,744,764 HSPA13
    nsv6549280copy number variation1nstd223human GRCh38 chr21: 14,372,469-14,373,096 , GRCh37.p13 chr21: 15,744,790-15,745,417 HSPA13
    nsv6547892copy number variation1nstd223human GRCh38 chr21: 14,382,601-14,384,300 , GRCh37.p13 chr21: 15,754,922-15,756,621 HSPA13, LOC105369304
    nsv6536080copy number variation1nstd223human GRCh38 chr21: 14,371,101-14,373,300 , GRCh37.p13 chr21: 15,743,422-15,745,621 HSPA13
    nsv6315551copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,420,615-48,080,926 , GRCh38.p12 chr21: 13,048,294-46,661,014 LTN1, LOC105372740, 622 more genes
    nsv6314187copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-28,820,583 , GRCh38.p12 chr21: 13,634,136-27,448,264 D21S2088E, MIR548XHG, 158 more genes
    nsv6314126copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-26,760,450 , GRCh38.p12 chr21: 13,634,136-25,388,138 FAM207CP, MIR125B2, 126 more genes
    nsv6314041copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-27,430,623 , GRCh38.p12 chr21: 13,634,136-26,058,307 SAMSN1-AS1, NRIP1, 142 more genes
    nsv6313951copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,041,209-48,097,372 , GRCh38.p12 chr21: 13,668,888-46,677,460 LOC107985515, ATP5PF, 606 more genes
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