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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3909037copy number variation1nstd102humanBenign GRCh37 chr20: 33,216,764-33,243,656 , GRCh38.p12 chr20: 34,628,960-34,655,852 PIGU
    nsv3905981copy number variation1nstd102humanBenign GRCh37 chr20: 33,240,403-33,243,656 , GRCh38.p12 chr20: 34,652,599-34,655,852 PIGU
    nsv7096022copy number variation1nstd102humanUncertain significance GRCh37 chr20: 33,222,399-33,222,539 , GRCh38.p12 chr20: 34,634,595-34,634,735 PIGU
    nsv3900101copy number variation1nstd102humanBenign GRCh37 chr20: 33,240,403-33,303,095 , GRCh38.p12 chr20: 34,652,599-34,715,291 PIGU, LOC105372599, 2 more genes
    nsv3896788copy number variation1nstd102humanBenign GRCh37 chr20: 33,242,326-33,303,095 , GRCh38.p12 chr20: 34,654,522-34,715,291 PIGU, TP53INP2, 2 more genes
    nsv3907682copy number variation1nstd102humanBenign GRCh37 chr20: 33,242,326-33,292,777 , GRCh38.p12 chr20: 34,654,522-34,704,973 PIGU, LOC105372599, 1 more genes
    nsv3912723copy number variation1nstd102humanPathogenic NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019 PIGU, LOC107985448, 370 more genes
    nsv3913594copy number variation1nstd102humanPathogenic GRCh37 chr20: 32,020,169-35,450,284 , NCBI36 chr20: 31,483,830-34,883,698 , GRCh38 chr20: 33,432,363-36,821,881 PIGU, AHCY, 93 more genes
    nsv6311078copy number variation1nstd102humanPathogenic GRCh37 chr20: 31,189,994-34,287,210 , GRCh38.p12 chr20: 32,602,192-35,699,288 PIGU, EDEM2, 93 more genes
    nsv3892750copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941 PIGU, TGIF2-RAB5IF, 1314 more genes
    nsv3905072copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435 PIGU, LRRN4, 1313 more genes
    nsv3895314copy number variation2nstd102humanPathogenic GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202 PIGU, PKIG, 1311 more genes
    nsv3896520copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110 PIGU, COMMD7, 1311 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 PIGU, MIR3646, 1310 more genes
    nsv3910142copy number variation1nstd102humanPathogenic GRCh37 chr20: 9,792,081-37,945,599 , GRCh38 chr20: 9,811,433-39,316,956 , NCBI36 chr20: 9,740,081-37,379,013 PIGU, DYNLRB1, 555 more genes
    nsv3918053copy number variation1nstd102humanPathogenic NCBI36 chr20: 25,703,100-38,491,480 , GRCh37.p13 chr20: 25,755,100-39,058,066 , GRCh38.p12 chr20: 25,774,464-40,429,426 PIGU, MYH7B, 300 more genes
    nsv6313956copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747 PIGU, LOC105372586, 193 more genes
    nsv4457806copy number variation1nstd102humanPathogenic GRCh37 chr20: 29,833,608-35,087,952 , GRCh38.p12 chr20: 31,245,805-36,459,549 PIGU, EFCAB8, 162 more genes
    nsv3920503copy number variation1nstd102humanPathogenic GRCh38 chr20: 32,062,768-35,906,606 , NCBI36 chr20: 30,114,232-33,957,942 , GRCh37 chr20: 30,650,571-34,494,528 PIGU, UQCC1, 111 more genes
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 PIGU, AHCY, 330 more genes
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