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Items: 1 to 20 of 39398

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3206953copy number variation1nstd152human GRCh38 chr1: 189,348,007-189,584,157 , GRCh37.p13 chr1: 189,317,137-189,553,287 LOC105371657
    nsv3190626copy number variation1nstd152human GRCh38 chr1: 189,348,007-189,584,157 , GRCh37.p13 chr1: 189,317,137-189,553,287 LOC105371657
    nsv3221307copy number variation3nstd152human GRCh38 chr11: 55,086,811-55,286,227 , GRCh37.p13 chr11: 54,854,287-55,053,703 TRIM48
    nsv3220797copy number variation2nstd152human GRCh38 chr7: 57,860,025-58,000,294 , GRCh37.p13 chr7: 57,919,731-58,054,331 LOC102723842
    nsv3198543copy number variation3nstd152human GRCh38 chr2: 80,945,501-81,081,366 , GRCh37.p13 chr2: 81,172,625-81,308,490 LOC105374827
    nsv3221600copy number variation9nstd152human GRCh38 chr11: 70,934,772-71,067,280 , GRCh37.p13 chr11|NW_004070871.1: 478,985-561,493 SHANK2
    nsv3190753copy number variation8nstd152human GRCh38 chr4: 21,075,739-21,206,721 , GRCh37.p13 chr4: 21,077,362-21,208,344 KCNIP4
    nsv3221159copy number variation9nstd152human GRCh38 chr15: 68,046,399-68,164,345 , GRCh37.p13 chr15: 68,338,737-68,456,683 PIAS1
    nsv3225831copy number variation2nstd152human GRCh38 chr11: 70,954,784-71,066,836 , GRCh37.p13 chr11|NW_004070871.1: 498,997-561,049 SHANK2
    nsv3204488copy number variation2nstd152human GRCh38 chr1: 169,183,581-169,288,506 , GRCh37.p13 chr1: 169,152,819-169,257,744 NME7
    nsv3218194copy number variation9nstd152human GRCh38 chr7: 96,824,384-96,919,001 , GRCh37.p13 chr7: 96,453,696-96,548,313 MARK2P10
    nsv3197073copy number variation3nstd152human GRCh38 chr2: 97,182,957-97,275,452 , GRCh37.p13 chr2: 97,848,694-97,941,189 ANKRD36
    nsv3190695copy number variation9nstd152human GRCh38 chr4: 180,895,149-180,984,192 , GRCh37.p13 chr4: 181,816,302-181,905,345 LOC105377568
    nsv3195581copy number variation9nstd152human GRCh38 chr6: 133,015,998-133,104,809 , GRCh37.p13 chr6: 133,337,137-133,425,948 LINC00326
    nsv3212441copy number variation3nstd152human GRCh38 chr9: 98,509,941-98,597,770 , GRCh37.p13 chr9: 101,272,223-101,360,052 GABBR2
    nsv3204797copy number variation3nstd152human GRCh38 chr2: 76,475,249-76,563,072 , GRCh37.p13 chr2: 76,702,375-76,790,198 LOC105374814
    nsv3213989copy number variation3nstd152human GRCh38 chr14: 41,126,665-41,207,973 , GRCh37.p13 chr14: 41,595,870-41,677,176 LINC02315
    nsv3196116copy number variation2nstd152human GRCh38 chr5: 83,914,143-83,995,367 , GRCh37.p13 chr5: 83,209,962-83,291,186 EDIL3
    nsv3201902copy number variation8nstd152human GRCh38 chr4: 49,083,235-49,161,472 , GRCh37.p13 chr4: 49,085,252-49,163,489 LOC101927209
    nsv3230221copy number variation9nstd152human GRCh38 chr11: 87,951,212-88,028,900 , GRCh37.p13 chr11: 87,662,104-87,762,068 RAB38
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