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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7048316inversion1nstd229human GRCh38 chr2: 217,690,925-222,070,373 , GRCh37.p13 chr2: 218,555,648-222,935,092 LOC105373895, CXCR2P1, 119 more genes
    nsv6691344copy number variation1nstd229human GRCh38 chr2: 218,676,186-218,676,532 , GRCh37.p13 chr2: 219,540,909-219,541,255 STK36
    nsv6690102copy number variation1nstd229human GRCh38 chr2: 218,455,001-218,684,900 , GRCh37.p13 chr2: 219,319,724-219,549,623 USP37, CNOT9, 8 more genes
    nsv6688373copy number variation1nstd229human GRCh38 chr2: 218,665,504-218,672,439 , GRCh37.p13 chr2: 219,530,227-219,537,162 STK36, RNF25
    nsv6685864copy number variation1nstd229human GRCh38 chr2: 216,932,763-218,687,760 , GRCh37.p13 chr2: 217,797,486-219,552,483 LOC105373872, IGFBP-AS1, 45 more genes
    nsv6678487copy number variation1nstd229human GRCh38 chr2: 218,699,345-218,701,862 , GRCh37.p13 chr2: 219,564,068-219,566,585 STK36
    nsv6343971copy number variation1nstd223human GRCh38 chr2: 218,676,892-218,681,369 , GRCh37.p13 chr2: 219,541,615-219,546,092 STK36
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313768copy number variation1nstd102humanUncertain significance GRCh37 chr2: 218,210,665-220,141,650 , GRCh38.p12 chr2: 217,345,942-219,276,928 PNKD, RNU6-136P, 73 more genes
    nsv6313686copy number variation1nstd102humanPathogenic GRCh37 chr2: 215,108,009-221,679,980 , GRCh38.p12 chr2: 214,243,285-220,815,260 BCS1L, LOC105373880, 160 more genes
    nsv6311374copy number variation2nstd102humanUncertain significance GRCh37 chr2: 218,999,525-220,435,954 , GRCh38.p12 chr2: 218,134,802-219,571,232 CHPF, WNT6, 83 more genes
    nsv5899521copy number variation1nstd209human GRCh38 chr2: 218,683,599-218,683,651 , GRCh37.p13 chr2: 219,548,322-219,548,374 STK36
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5539836insertion1nstd206human GRCh38 chr2: 218,682,967-218,682,967 , GRCh37.p13 chr2: 219,547,690-219,547,690 STK36
    nsv5165580mobile element insertion1nstd203human GRCh38 chr2: 218,681,577-218,681,588 , GRCh37.p13 chr2: 219,546,300-219,546,311 STK36
    nsv5029880inversion1nstd200human GRCh38 chr2: 213,444,845-219,177,092 , GRCh37.p13 chr2: 214,309,569-220,041,814 , LOC102724861, 122 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4728446copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 215,122,019-220,397,907 , GRCh38.p12 chr2: 214,257,295-219,533,185 AAMP, ATIC, 139 more genes
    nsv4673965copy number variation1nstd102humanPathogenic GRCh37 chr2: 216,883,237-220,953,003 , GRCh38.p12 chr2: 216,018,514-220,088,282 LOC105373887, STK11IP, 138 more genes
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