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Items: 1 to 20 of 23

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4730014copy number variation1nstd102humanUncertain significance GRCh37 chr19: 31,911,128-32,233,752 , GRCh38.p12 chr19: 31,420,222-31,742,846 LOC105372361, TSHZ3-AS1, 3 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 TSHZ3, UBA2, 241 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 TSHZ3, MAG, 238 more genes
    nsv3918197copy number variation1nstd102humanPathogenic GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000 LINC01531, FXYD5, 110 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 TSHZ3, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 TSHZ3, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 TSHZ3, LENG8, 2408 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 TSHZ3, BCKDHA, 1102 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 TSHZ3, ZNF420, 574 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 TSHZ3, ZNF461, 735 more genes
    nsv3914228copy number variation1nstd102humanPathogenic NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054 TSHZ3, LOC105372355, 411 more genes
    nsv3900139copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,735,448-36,120,396 , GRCh38.p12 chr19: 30,244,541-35,629,494 TSHZ3, ZNF599, 130 more genes
    nsv3920776copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 34,234,635-37,150,342 , GRCh37 chr19: 29,542,795-32,458,502 , GRCh38 chr19: 29,051,888-31,967,596 TSHZ3, CCNE1, 30 more genes
    nsv3903946copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 30,112,378-31,939,682 , GRCh38.p12 chr19: 29,621,471-31,448,776 TSHZ3, CCNE1, 17 more genes
    nsv3921610copy number variation1nstd102humanBenign NCBI36 chr19: 35,779,270-36,476,428 , GRCh37 chr19: 31,087,430-31,784,588 , GRCh38 chr19: 30,596,523-31,293,682 TSHZ3, LOC105372355, 6 more genes
    nsv3918395copy number variation1nstd102humanUncertain significance NCBI36 chr19: 36,125,407-36,748,049 , GRCh37.p13 chr19: 31,433,567-32,056,209 , GRCh38.p12 chr19: 30,942,661-31,565,303 TSHZ3, LOC105372356, 5 more genes
    nsv3904271copy number variation1nstd102humanUncertain significance GRCh37 chr19: 31,792,864-32,335,982 , GRCh38.p12 chr19: 31,301,958-31,845,076 TSHZ3, LINC01837, 7 more genes
    nsv4457781copy number variation1nstd102humanUncertain significance GRCh37 chr19: 30,741,915-32,212,809 , GRCh38.p12 chr19: 30,251,008-31,721,903 TSHZ3, LOC105372355, 11 more genes
    nsv4729966copy number variation1nstd102humanUncertain significance GRCh37 chr19: 31,532,896-32,341,833 , GRCh38.p12 chr19: 31,041,990-31,850,927 TSHZ3, RNA5SP471, 10 more genes
    nsv4730004copy number variation1nstd102humanUncertain significance GRCh37 chr19: 31,051,497-31,804,809 , GRCh38.p12 chr19: 30,560,590-31,313,903 TSHZ3, LOC105372355, 6 more genes
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