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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4674258copy number variation1nstd102humanUncertain significance GRCh37 chr2: 165,676,080-165,768,131 , GRCh38.p12 chr2: 164,819,570-164,911,621 SLC38A11, RNA5SP110, 3 more genes
    nsv3924630copy number variation1nstd102humanUncertain significance NCBI36 chr2: 165,325,777-165,471,119 , GRCh37.p13 chr2: 165,617,531-165,762,873 , GRCh38.p12 chr2: 164,761,021-164,906,363 SLC38A11, LOC101929633, 3 more genes
    nsv3918451copy number variation1nstd102humanPathogenic NCBI36 chr2: 165,325,777-165,973,710 , GRCh37.p13 chr2: 165,617,531-166,265,464 , GRCh38.p12 chr2: 164,761,021-165,408,954 SLC38A11, SCN2A, 6 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 SLC38A11, DAZAP2P1, 2991 more genes
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 SLC38A11, RBM45, 258 more genes
    nsv3904056copy number variation1nstd102humanPathogenic GRCh37 chr2: 164,821,892-183,059,789 , NCBI36 chr2: 164,530,138-182,768,034 , GRCh38 chr2: 163,965,382-182,195,062 SLC38A11, PRKRA, 256 more genes
    nsv6315160copy number variation1nstd102humanPathogenic GRCh37 chr2: 160,347,642-174,075,851 , GRCh38.p12 chr2: 159,491,131-173,211,123 SLC38A11, EIF3EP3, 158 more genes
    nsv3877758copy number variation1nstd102humanPathogenic GRCh37 chr2: 157,970,774-169,270,675 , GRCh38.p12 chr2: 157,114,262-168,414,165 SLC38A11, GCA, 121 more genes
    nsv3909452copy number variation1nstd102humanPathogenic GRCh37 chr2: 165,706,627-176,423,918 , GRCh38 chr2: 164,850,117-175,559,190 , NCBI36 chr2: 165,414,873-176,132,164 SLC38A11, LOC107985959, 141 more genes
    nsv3904389copy number variation1nstd102humanPathogenic GRCh38 chr2: 158,382,388-166,605,758 , GRCh37 chr2: 159,238,900-167,462,268 , NCBI36 chr2: 158,947,146-167,170,514 SLC38A11, TANC1, 95 more genes
    nsv3903934copy number variation1nstd102humanPathogenic GRCh37 chr2: 164,922,548-172,962,614 , NCBI36 chr2: 164,630,794-172,670,860 , GRCh38 chr2: 164,066,038-172,097,886 SLC38A11, LOC105373739, 95 more genes
    nsv6313780copy number variation1nstd102humanPathogenic GRCh37 chr2: 161,551,326-167,762,790 , GRCh38.p12 chr2: 160,694,815-166,906,280 SLC38A11, SCN9A, 60 more genes
    nsv4346986copy number variation1nstd102humanPathogenic GRCh37 chr2: 162,485,583-168,295,583 , GRCh38.p12 chr2: 161,629,073-167,439,073 SLC38A11, CYP2C56P, 49 more genes
    nsv3920656copy number variation1nstd102humanPathogenic NCBI36 chr2: 164,217,738-169,989,662 , GRCh37.p13 chr2: 164,509,492-170,281,416 , GRCh38.p12 chr2: 163,652,982-169,424,906 SLC38A11, RNU6-766P, 48 more genes
    nsv3887115copy number variation1nstd102humanPathogenic GRCh37 chr2: 164,366,067-169,069,454 , GRCh38.p12 chr2: 163,509,557-168,212,944 SLC38A11, EIF3EP3, 32 more genes
    nsv3907730copy number variation1nstd102humanPathogenic NCBI36 chr2: 164,020,046-167,527,078 , GRCh37 chr2: 164,311,800-167,818,832 , GRCh38 chr2: 163,455,290-166,962,322 SLC38A11, FIGN, 28 more genes
    nsv6313838copy number variation1nstd102humanPathogenic GRCh37 chr2: 165,428,510-166,888,012 , GRCh38.p12 chr2: 164,572,000-166,031,502 SLC38A11, RNA5SP111, 16 more genes
    nsv6313535copy number variation1nstd102humanPathogenic GRCh38.p12 chr2: 164,938,048-165,777,365 , GRCh37 chr2: 165,794,558-166,633,875 SLC38A11, GALNT3, 4 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 SLC38A11, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 SLC38A11, IGKV2OR2-10, 3737 more genes
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