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Items: 1 to 20 of 585

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099260copy number variation1nstd231human GRCh38.p12 chr1: 207,518,788-210,916,265 , GRCh37 chr1: 207,692,133-211,089,607 ADORA2BP1, ATP5MC2P1, 60 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7046111inversion1nstd229human GRCh38 chr1: 207,240,836-207,500,601 , GRCh37.p13 chr1: 207,414,181-207,673,946 CD55, CR1, 2 more genes
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv6677264copy number variation1nstd229human GRCh38 chr1: 207,596,493-207,601,786 , GRCh37.p13 chr1: 207,769,838-207,775,131 CR1
    nsv6675041copy number variation1nstd229human GRCh38 chr1: 207,635,151-207,637,063 , GRCh37.p13 chr1: 207,808,496-207,810,408 CR1
    nsv6674862copy number variation1nstd229human GRCh38 chr1: 207,582,374-207,590,875 , GRCh37.p13 chr1: 207,755,719-207,764,220 CR1
    nsv6673288copy number variation1nstd229human GRCh38 chr1: 207,581,139-207,581,352 , GRCh37.p13 chr1: 207,754,484-207,754,697 CR1
    nsv6670419copy number variation1nstd229human GRCh38 chr1: 207,565,801-207,572,200 , GRCh37.p13 chr1: 207,739,146-207,745,545 CR1
    nsv6668550copy number variation1nstd229human GRCh38 chr1: 207,632,401-207,749,300 , GRCh37.p13 chr1: 207,805,746-207,922,645 CR1, CDCA4P3, 4 more genes
    nsv6667545copy number variation1nstd229human GRCh38 chr1: 207,619,465-207,619,898 , GRCh37.p13 chr1: 207,792,810-207,793,243 CR1
    nsv6667542copy number variation1nstd229human GRCh38 chr1: 207,594,815-207,600,160 , GRCh37.p13 chr1: 207,768,160-207,773,505 CR1
    nsv6666302copy number variation1nstd229human GRCh38 chr1: 207,575,776-207,577,366 , GRCh37.p13 chr1: 207,749,121-207,750,711 CR1
    nsv6666075copy number variation1nstd229human GRCh38 chr1: 207,500,090-207,500,131 , GRCh37.p13 chr1: 207,673,435-207,673,476 CR1
    nsv6662748copy number variation1nstd229human GRCh38 chr1: 207,631,282-207,693,384 , GRCh37.p13 chr1: 207,804,627-207,866,729 CDCA4P3, CR1, 2 more genes
    nsv6661443copy number variation1nstd229human GRCh38 chr1: 207,603,875-207,606,701 , GRCh37.p13 chr1: 207,777,220-207,780,046 CR1
    nsv6660406copy number variation1nstd229human GRCh38 chr1: 207,601,502-207,612,972 , GRCh37.p13 chr1: 207,774,847-207,786,317 CR1
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6554773inversion1nstd223human GRCh38 chr1: 204,500,842-208,290,127 , GRCh37.p13 chr1: 204,469,970-208,463,472 RNA5SP75, LOC105372869, 108 more genes
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