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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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 ARL4C, DAZAP2P1, 2991 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 ARL4C, LOC105373947, 357 more genes
    nsv3898929copy number variation2nstd102humanPathogenic GRCh38 chr2: 231,770,279-242,126,245 , GRCh37 chr2: 232,634,989-243,059,659 , NCBI36 chr2: 232,343,233-242,717,069 ARL4C, PDE6D, 227 more genes
    nsv3893827copy number variation1nstd102humanPathogenic NCBI36 chr2: 227,551,089-237,459,981 , GRCh38 chr2: 226,978,129-236,886,599 , GRCh37 chr2: 227,842,845-237,795,242 ARL4C, B3GNT7, 193 more genes
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 ARL4C, LOC107985836, 217 more genes
    nsv6315436copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,227,837-242,783,384 , GRCh38.p12 chr2: 232,363,127-241,841,232 ARL4C, LOC105373929, 204 more genes
    nsv3871027copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,784,243-243,040,217 , GRCh38.p12 chr2: 232,919,533-242,098,066 ARL4C, MROH2A, 194 more genes
    nsv3910501copy number variation1nstd102humanPathogenic NCBI36 chr2: 233,599,457-242,717,007 , GRCh37.p13 chr2: 233,891,213-243,068,334 , GRCh38.p12 chr2: 233,026,503-242,126,183 ARL4C, UGT1A3, 194 more genes
    nsv3894767copy number variation1nstd102humanPathogenic GRCh38 chr2: 233,420,162-242,086,301 , NCBI36 chr2: 233,704,084-242,677,125 , GRCh37 chr2: 233,995,840-243,028,452 ARL4C, LOC112268433, 184 more genes
    nsv3892808copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,362,257-243,041,306 , NCBI36 chr2: 234,026,996-242,689,979 , GRCh38 chr2: 233,453,611-242,099,155 ARL4C, RPL3P5, 185 more genes
    nsv3877071copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,495,262-242,783,384 , GRCh38.p12 chr2: 233,586,616-241,841,232 ARL4C, RNU6-1140P, 171 more genes
    nsv3906029copy number variation1nstd102humanPathogenic NCBI36 chr2: 227,916,238-235,912,551 , GRCh38 chr2: 227,343,278-235,339,168 , GRCh37 chr2: 228,207,994-236,247,812 ARL4C, SP110, 167 more genes
    nsv4674624copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,791,927-242,783,384 , GRCh38.p12 chr2: 233,883,281-241,841,232 ARL4C, LOC93463, 151 more genes
    nsv3899818copy number variation1nstd102humanPathogenic NCBI36 chr2: 234,745,919-242,677,125 , GRCh37 chr2: 235,081,180-243,028,452 , GRCh38 chr2: 234,172,536-242,086,301 ARL4C, SCLY, 159 more genes
    nsv3907279copy number variation1nstd102humanPathogenic GRCh37 chr2: 235,254,486-243,059,659 , GRCh38 chr2: 234,345,842-242,126,245 , NCBI36 chr2: 234,919,225-242,717,069 ARL4C, LINC01937, 159 more genes
    nsv3892556copy number variation1nstd102humanPathogenic GRCh37 chr2: 235,068,297-242,783,384 , NCBI36 chr2: 234,733,036-242,432,057 , GRCh38 chr2: 234,159,653-241,841,232 ARL4C, OR6B2, 149 more genes
    nsv6313683copy number variation1nstd102humanPathogenic GRCh37 chr2: 228,807,574-235,475,892 , GRCh38.p12 chr2: 227,942,858-234,567,248 ARL4C, RNU7-9P, 143 more genes
    nsv4674274copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,090,049-239,494,702 , GRCh38.p12 chr2: 233,181,403-238,586,061 ARL4C, LOC105373933, 105 more genes
    nsv3892064copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,967,401-240,365,384 , NCBI36 chr2: 234,632,140-240,030,321 , GRCh38 chr2: 234,058,757-239,443,690 ARL4C, LOC105373949, 87 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 ARL4C, LOC112268439, 3737 more genes
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