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Items: 1 to 20 of 26

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3909261copy number variation1nstd102humanBenign GRCh37 chr6: 152,387,664-152,392,561 , GRCh38.p12 chr6: 152,066,529-152,071,426 ESR1
    nsv3896315copy number variation1nstd102humanBenign GRCh37 chr6: 152,389,968-152,392,561 , GRCh38.p12 chr6: 152,068,833-152,071,426 ESR1
    nsv3905142copy number variation1nstd102humanBenign GRCh37 chr6: 152,389,968-152,392,174 , GRCh38.p12 chr6: 152,068,833-152,071,039 ESR1
    nsv3904937copy number variation1nstd102humanBenign GRCh37 chr6: 152,390,058-152,392,174 , GRCh38.p12 chr6: 152,068,923-152,071,039 ESR1
    nsv4456174copy number variation1nstd102humanUncertain significance GRCh37 chr6: 152,017,744-152,031,586 , GRCh38.p12 chr6: 151,696,609-151,710,451 ESR1
    nsv4456216copy number variation1nstd102humanUncertain significance GRCh37 chr6: 152,209,421-152,645,055 , GRCh38.p12 chr6: 151,888,286-152,323,920 ESR1, SYNE1
    nsv4452614copy number variation1nstd102humanUncertain significance GRCh37 chr6: 152,443,551-152,534,914 , GRCh38 chr6: 152,122,416-152,213,779 ESR1, SYNE1
    nsv3916405copy number variation1nstd102humanPathogenic NCBI36 chr6: 150,744,068-159,894,974 , GRCh38 chr6: 150,381,239-159,553,952 , GRCh37 chr6: 150,702,375-159,974,984 ESR1, LOC112267968, 126 more genes
    nsv3890752copy number variation1nstd102humanPathogenic GRCh37 chr6: 144,075,695-152,337,005 , GRCh38.p12 chr6: 143,754,558-152,015,870 ESR1, LOC105378052, 109 more genes
    nsv3920651copy number variation1nstd102humanPathogenic GRCh38 chr6: 144,932,561-152,985,364 , NCBI36 chr6: 145,295,390-153,348,192 , GRCh37 chr6: 145,253,697-153,306,499 ESR1, PPP1R14C, 107 more genes
    nsv7148221copy number variation1nstd102humanPathogenic GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958 ESR1, RNU6-824P, 97 more genes
    nsv4675234copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929 ESR1, RNU7-3P, 86 more genes
    nsv3882645copy number variation1nstd102humanPathogenic GRCh37 chr6: 152,443,551-153,748,051 , GRCh38 chr6: 152,122,416-153,426,916 ESR1, LOC107986661, 18 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 ESR1, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 ESR1, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 ESR1, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ESR1, ITPR3, 2905 more genes
    nsv3911993copy number variation1nstd102humanPathogenic NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033 ESR1, LOC105369171, 418 more genes
    nsv3915150copy number variation1nstd102humanPathogenic NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038 ESR1, KATNA1, 422 more genes
    nsv3920975copy number variation1nstd102humanPathogenic GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591 ESR1, UST-AS2, 394 more genes
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