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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099266copy number variation1nstd231human GRCh38.p12 chr1: 226,993,371-235,936,592 , GRCh37 chr1: 227,181,072-236,099,892 ACTA1, AGT, 223 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7054589inversion1nstd229human GRCh38 chr1: 227,539,174-227,767,032 , GRCh37.p13 chr1: 227,726,875-227,954,733 ZNF678, MRPL57P2, 6 more genes
    nsv7046952inversion1nstd229human GRCh38 chr1: 227,416,479-227,774,357 , GRCh37.p13 chr1: 227,604,180-227,962,058 RPS18P3, BTF3P9, 12 more genes
    nsv7043468inversion1nstd229human GRCh38 chr1: 227,499,586-227,807,528 , GRCh37.p13 chr1: 227,687,287-227,995,229 ZNF678, SNAP47, 9 more genes
    nsv6677148copy number variation1nstd229human GRCh38 chr1: 227,767,271-227,771,387 , GRCh37.p13 chr1: 227,954,972-227,959,088 SNAP47
    nsv6676346copy number variation1nstd229human GRCh38 chr1: 227,739,342-227,739,431 , GRCh37.p13 chr1: 227,927,043-227,927,132 SNAP47
    nsv6675391copy number variation1nstd229human GRCh38 chr1: 227,593,979-227,749,286 , GRCh37.p13 chr1: 227,781,680-227,936,987 FAM133FP, ZNF678, 4 more genes
    nsv6671687copy number variation1nstd229human GRCh38 chr1: 227,714,303-227,737,701 , GRCh37.p13 chr1: 227,902,004-227,925,402 SNAP47, JMJD4
    nsv6670489copy number variation1nstd229human GRCh38 chr1: 227,575,489-231,747,964 , GRCh37.p13 chr1: 227,763,190-231,883,710 FAM89A, RNA5S14, 127 more genes
    nsv6669964copy number variation1nstd229human GRCh38 chr1: 227,749,760-227,749,819 , GRCh37.p13 chr1: 227,937,461-227,937,520 SNAP47
    nsv6665826copy number variation1nstd229human GRCh38 chr1: 227,754,936-227,758,521 , GRCh37.p13 chr1: 227,942,637-227,946,222 SNAP47
    nsv6658656copy number variation1nstd229human GRCh38 chr1: 227,662,731-227,731,913 , GRCh37.p13 chr1: 227,850,432-227,919,614 ZNF678, JMJD4, 2 more genes
    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
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636347copy number variation1nstd102humanUncertain significance GRCh37 chr1: 227,696,110-227,993,585 , GRCh38.p12 chr1: 227,508,409-227,805,884 ZNF847P, LOC105373289, 9 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
    nsv6551408inversion1nstd223human GRCh38 chr1: 227,499,583-227,807,531 , GRCh37.p13 chr1: 227,687,284-227,995,232 ZNF847P, RNA5SP77, 9 more genes
    nsv6549532inversion1nstd223human GRCh38 chr1: 227,777,056-227,779,316 , GRCh37.p13 chr1: 227,964,757-227,967,017 SNAP47
    nsv6332892copy number variation1nstd223human GRCh38 chr1: 227,743,471-227,743,793 , GRCh37.p13 chr1: 227,931,172-227,931,494 SNAP47
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