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Items: 1 to 20 of 198

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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
    nsv7095780copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 209,803,072-209,812,003 , GRCh38.p12 chr1: 209,629,727-209,638,658 LAMB3
    nsv7095779copy number variation1nstd102humanPathogenic GRCh37 chr1: 209,788,514-209,825,713 , GRCh38.p12 chr1: 209,615,169-209,652,368 MIR4260, LAMB3
    nsv7093149copy number variation1nstd102humanPathogenic GRCh37 chr1: 209,795,923-209,795,924 , GRCh38 chr1: 209,622,578-209,622,579 LAMB3, MIR4260
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv6675568copy number variation1nstd229human GRCh38 chr1: 209,643,697-209,643,752 , GRCh37.p13 chr1: 209,817,042-209,817,097 LAMB3
    nsv6670977copy number variation1nstd229human GRCh38 chr1: 209,637,187-209,643,958 , GRCh37.p13 chr1: 209,810,532-209,817,303 LAMB3
    nsv6668935copy number variation1nstd229human GRCh38 chr1: 209,630,979-209,710,969 , GRCh37.p13 chr1: 209,804,324-209,884,314 G0S2, HSD11B1, 2 more genes
    nsv6661296copy number variation1nstd229human GRCh38 chr1: 209,629,834-209,629,911 , GRCh37.p13 chr1: 209,803,179-209,803,256 LAMB3
    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
    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
    nsv6626084copy number variation1nstd224human GRCh37 chr1: 209,621,776-210,982,084 , GRCh38.p12 chr1: 209,448,431-210,808,742 IRF6, TRAF3IP3, 23 more genes
    nsv6325553copy number variation1nstd223human GRCh38 chr1: 209,453,567-212,914,449 , GRCh37.p13 chr1: 209,626,912-213,087,791 ST13P19, RPS5P4, 74 more genes
    nsv6322260copy number variation1nstd223human GRCh38 chr1: 209,640,558-209,641,082 , GRCh37.p13 chr1: 209,813,903-209,814,427 LAMB3
    nsv6321267copy number variation1nstd223human GRCh38 chr1: 209,345,386-209,677,728 , GRCh37.p13 chr1: 209,518,731-209,851,073 HSD11B1-AS1, LOC105372898, 9 more genes
    nsv6133752copy number variation1nstd213human GRCh37 chr1: 207,160,000-210,270,001 , GRCh38.p12 chr1: 206,986,655-210,096,656 ADORA2BP1, C4BPA, 62 more genes
    nsv6133630copy number variation2nstd213human GRCh37 chr1: 206,490,000-223,720,001 , GRCh38.p12 chr1: 206,316,655-223,546,636 ATP5MC2P1, CENPF, 269 more genes
    nsv5673315copy number variation1nstd102humanPathogenic GRCh37 chr1: 209,798,983-209,812,003 , GRCh38.p12 chr1: 209,625,638-209,638,658 LAMB3
    nsv5610013insertion1nstd207human GRCh38 chr1: 209,626,459-209,626,459 , GRCh37.p13 chr1: 209,799,804-209,799,804 LAMB3
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