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Items: 1 to 20 of 755

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138475copy number variation1nstd232human GRCh37.p13 chr22: 40,935,460-40,935,622 , GRCh38.p12 chr22: 40,539,456-40,539,618 MRTFA
    nsv7096312copy number variation1nstd102humanUncertain significance GRCh37 chr22: 40,741,451-40,859,231 , GRCh38.p12 chr22: 40,345,447-40,463,227 SGSM3-AS1, ADSL, 2 more genes
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7077764inversion1nstd229human GRCh38 chr22: 37,971,370-41,589,449 , GRCh37.p13 chr22: 38,367,377-41,985,453 UQCRFS1P1, LOC105373027, 119 more genes
    nsv7074321inversion1nstd229human GRCh38 chr22: 40,474,466-40,474,519 , GRCh37.p13 chr22: 40,870,470-40,870,523 MRTFA
    nsv7070838inversion1nstd229human GRCh38 chr22: 40,481,826-41,015,795 , GRCh37.p13 chr22: 40,877,830-41,411,799 RFKP4, COX6B1P3, 14 more genes
    nsv7067082inversion1nstd229human GRCh38 chr22: 40,413,137-40,413,390 , GRCh37.p13 chr22: 40,809,141-40,809,394 MRTFA
    nsv7064338inversion1nstd229human GRCh38 chr22: 40,322,864-40,533,291 , GRCh37.p13 chr22: 40,718,868-40,929,295 ADSL, SGSM3, 4 more genes
    nsv7063409inversion1nstd229human GRCh38 chr22: 40,412,982-40,413,503 , GRCh37.p13 chr22: 40,808,986-40,809,507 MRTFA
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7037682copy number variation1nstd229human GRCh38 chr22: 40,475,901-40,484,900 , GRCh37.p13 chr22: 40,871,905-40,880,904 MRTFA
    nsv7037672copy number variation1nstd229human GRCh38 chr22: 40,446,201-40,449,200 , GRCh37.p13 chr22: 40,842,205-40,845,204 MRTFA
    nsv7037373copy number variation1nstd229human GRCh38 chr22: 40,439,332-40,447,502 , GRCh37.p13 chr22: 40,835,336-40,843,506 MRTFA
    nsv7035637copy number variation1nstd229human GRCh38 chr22: 40,420,532-40,420,662 , GRCh37.p13 chr22: 40,816,536-40,816,666 MRTFA
    nsv7033741copy number variation1nstd229human GRCh38 chr22: 40,495,541-40,543,497 , GRCh37.p13 chr22: 40,891,545-40,939,501 MRTFA-AS1, MRTFA
    nsv7031634copy number variation1nstd229human GRCh38 chr22: 40,410,282-40,410,408 , GRCh37.p13 chr22: 40,806,286-40,806,412 SGSM3, MRTFA
    nsv7031629copy number variation1nstd229human GRCh38 chr22: 40,477,203-40,484,922 , GRCh37.p13 chr22: 40,873,207-40,880,926 MRTFA
    nsv7028504copy number variation1nstd229human GRCh38 chr22: 40,489,734-40,492,173 , GRCh37.p13 chr22: 40,885,738-40,888,177 MRTFA
    nsv7028442copy number variation1nstd229human GRCh38 chr22: 40,503,666-40,508,747 , GRCh37.p13 chr22: 40,899,670-40,904,751 MRTFA
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