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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099262copy number variation1nstd231human GRCh38.p12 chr1: 211,826,028-221,140,287 , GRCh37 chr1: 211,999,370-221,313,629 ATF3, CENPF, 114 more genes
    nsv7093375copy number variation1nstd102humannot provided GRCh37 chr1: 217,923,165-218,542,059 , GRCh38.p12 chr1: 217,749,823-218,368,717 LINC01653, LINC00210, 10 more genes
    nsv7054856inversion1nstd229human GRCh38 chr1: 217,869,263-217,918,660 , GRCh37.p13 chr1: 218,042,605-218,092,002 LINC00210, LOC105372922, 1 more genes
    nsv7052137inversion1nstd229human GRCh38 chr1: 217,890,301-217,919,306 , GRCh37.p13 chr1: 218,063,643-218,092,648 LOC105372922, LINC00210
    nsv6675880copy number variation1nstd229human GRCh38 chr1: 217,901,510-217,901,534 , GRCh37.p13 chr1: 218,074,852-218,074,876 LINC00210
    nsv6670037copy number variation1nstd229human GRCh38 chr1: 217,814,587-218,303,167 , GRCh37.p13 chr1: 217,987,929-218,476,509 UBBP2, LINC01653, 6 more genes
    nsv6668105copy number variation1nstd229human GRCh38 chr1: 217,903,301-218,032,700 , GRCh37.p13 chr1: 218,076,643-218,206,042 LOC105372922, LINC00210
    nsv6665702copy number variation1nstd229human GRCh38 chr1: 217,901,965-217,905,445 , GRCh37.p13 chr1: 218,075,307-218,078,787 LINC00210
    nsv6664576copy number variation1nstd229human GRCh38 chr1: 217,911,301-217,918,000 , GRCh37.p13 chr1: 218,084,643-218,091,342 LINC00210, LOC105372922
    nsv6660209copy number variation1nstd229human GRCh38 chr1: 217,903,286-217,903,981 , GRCh37.p13 chr1: 218,076,628-218,077,323 LINC00210
    nsv6659587copy number variation1nstd229human GRCh38 chr1: 217,909,321-217,909,555 , GRCh37.p13 chr1: 218,082,663-218,082,897 LINC00210
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 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
    nsv6544707inversion1nstd223human GRCh38 chr1: 217,900,597-217,900,722 , GRCh37.p13 chr1: 218,073,939-218,074,064 LINC00210
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
    nsv6327163copy number variation1nstd223human GRCh38 chr1: 217,814,587-218,303,167 , GRCh37.p13 chr1: 217,987,929-218,476,509 SPATA17, LINC01653, 6 more genes
    nsv6317612copy number variation1nstd223human GRCh38 chr1: 217,909,321-217,909,555 , GRCh37.p13 chr1: 218,082,663-218,082,897 LINC00210
    nsv6313524copy number variation1nstd102humanUncertain significance GRCh37 chr1: 216,767,549-218,152,575 , GRCh38.p12 chr1: 216,594,207-217,979,233 SPATA17, LINC00210, 7 more genes
    nsv6290633copy number variation1nstd102humanPathogenic GRCh37 chr1: 217,589,671-219,026,274 , GRCh38.p12 chr1: 217,416,329-218,852,932 LINC01653, SPATA17-AS1, 15 more genes
    nsv6290612copy number variation1nstd102humanPathogenic GRCh37 chr1: 216,243,817-220,231,236 , GRCh38.p12 chr1: 216,070,475-220,057,894 LINC00210, LOC107985281, 36 more genes
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