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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3879343copy number variation1nstd102humanBenign GRCh37 chr2: 216,923,679-217,006,039 , GRCh38.p12 chr2: 216,058,956-216,141,316 PECR, TMEM169, 1 more genes
    nsv3917579copy number variation1nstd102humanUncertain significance NCBI36 chr2: 216,481,622-216,647,549 , GRCh37.p13 chr2: 216,773,377-216,939,304 , GRCh38.p12 chr2: 215,908,654-216,074,581 PECR, LOC105373870, 1 more genes
    nsv4449802copy number variation1nstd102humanUncertain significance GRCh37 chr2: 216,937,755-217,001,750 , GRCh38.p12 chr2: 216,073,032-216,137,027 PECR, TMEM169, 1 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 PECR, DAZAP2P1, 2991 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 PECR, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 PECR, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 PECR, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 PECR, MTND2P22, 3724 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 PECR, LOC105376755, 1013 more genes
    nsv3890898copy number variation1nstd102humanPathogenic GRCh38 chr2: 188,818,195-242,065,208 , NCBI36 chr2: 189,391,166-242,656,032 , GRCh37 chr2: 189,682,921-243,007,359 PECR, LOC105373909, 901 more genes
    nsv3896499copy number variation1nstd102humanPathogenic GRCh37 chr2: 190,300,875-242,783,384 , NCBI36 chr2: 190,009,120-242,432,057 , GRCh38 chr2: 189,436,149-241,841,232 PECR, RNU6-1206P, 883 more genes
    nsv3908112copy number variation1nstd102humanPathogenic GRCh38 chr2: 190,310,736-241,892,770 , NCBI36 chr2: 190,883,707-242,483,594 , GRCh37 chr2: 191,175,462-242,834,921 PECR, LOC101928084, 871 more genes
    nsv3902143copy number variation1nstd102humanPathogenic GRCh38 chr2: 180,513,793-224,302,848 , NCBI36 chr2: 181,086,765-224,875,809 , GRCh37 chr2: 181,378,520-225,167,565 PECR, LINC00607, 644 more genes
    nsv3892046copy number variation1nstd102humanPathogenic GRCh37 chr2: 195,763,507-237,382,556 , NCBI36 chr2: 195,471,752-237,047,295 , GRCh38 chr2: 194,898,783-236,473,913 PECR, NPM1P46, 706 more genes
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 PECR, DNAJB1P1, 580 more genes
    nsv4436532copy number variation1nstd102humanPathogenic GRCh37 chr2: 188,926,928-225,298,653 , GRCh38.p12 chr2: 188,062,201-224,433,936 PECR, MARS2, 575 more genes
    nsv3892823copy number variation1nstd102humanPathogenic GRCh37 chr2: 211,444,400-243,059,659 , GRCh38 chr2: 210,579,676-242,126,245 , NCBI36 chr2: 211,152,645-242,717,069 PECR, RPL19P5, 567 more genes
    nsv3871121copy number variation1nstd102humanPathogenic GRCh37 chr2: 213,518,431-242,783,384 , GRCh38.p12 chr2: 212,653,707-241,841,232 PECR, TWIST2, 544 more genes
    nsv4435891copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,779,657-239,879,183 , GRCh38.p12 chr2: 209,914,933-238,957,487 PECR, XRCC5, 494 more genes
    nsv3889455copy number variation1nstd102humanPathogenic GRCh37 chr2: 205,169,148-219,149,293 , GRCh38.p12 chr2: 204,304,425-218,284,570 PECR, RPL37A, 188 more genes
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