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Items: 1 to 20 of 3568

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5555939sequence alteration1nstd206human GRCh38 chr18: 71,913,791-72,260,374 , GRCh37.p13 chr18: 69,581,027-69,927,609 LOC105372189
    nsv5558534sequence alteration1nstd206human GRCh38 chr22: 11,285,958-11,597,527 , GRCh37.p13 chr: NaN-NaN ZNF73P
    nsv5559528sequence alteration1nstd206human GRCh38 chr3: 78,327,401-78,585,274 , GRCh37.p13 chr3: 78,376,551-78,634,424 MRPS17P3
    nsv5562666sequence alteration1nstd206human GRCh38 chr5: 61,909,570-62,107,287 , GRCh37.p13 chr5: 61,205,397-61,403,114 LOC105378998
    nsv5563914sequence alteration1nstd206human GRCh38 chr7: 152,877,681-153,063,024 , GRCh37.p13 chr7: 152,574,766-152,760,109 ACTR3B
    nsv5555313sequence alteration1nstd206human GRCh38 chr9: 11,692,195-11,862,598 , GRCh37.p13 chr9: 11,692,195-11,862,598 LOC101929446
    nsv5561840sequence alteration1nstd206human GRCh38 chr2: 123,021,058-123,176,398 , GRCh37.p13 chr2: 123,778,634-123,933,974 LINC01826
    nsv5555813sequence alteration1nstd206human GRCh38 chr7: 109,654,790-109,791,530 , GRCh37.p13 chr7: 109,294,847-109,431,587 LOC100421901
    nsv5555914sequence alteration1nstd206human GRCh38 chr1: 189,885,472-190,021,353 , GRCh37.p13 chr1: 189,854,602-189,990,483 LOC647132
    nsv5563482sequence alteration1nstd206human GRCh38 chr2: 100,760,576-100,882,484 , GRCh37.p13 chr2: 101,377,038-101,498,946 NPAS2
    nsv5562834sequence alteration1nstd206human GRCh38 chrY: 19,066,442-19,177,974 , GRCh37.p13 chrY: 21,228,328-21,339,860 TTTY14
    nsv5558008sequence alteration1nstd206human GRCh38 chr4: 75,291,396-75,385,331 , GRCh37.p13 chr4: 76,216,606-76,310,541 LINC02483
    nsv5561520sequence alteration1nstd206human GRCh38 chr7: 119,864,737-119,955,474 , GRCh37.p13 chr7: 119,504,791-119,595,528 LINC02476
    nsv5554250sequence alteration1nstd206human GRCh38 chr4: 34,709,300-34,799,476 , GRCh37.p13 chr4: 34,710,922-34,801,098 LOC105378262
    nsv5558127sequence alteration1nstd206human GRCh38 chr22: 39,203,466-39,293,496 , GRCh37.p13 chr22: 39,599,471-39,689,501 PDGFB
    nsv5558999sequence alteration1nstd206human GRCh38 chr2: 187,946,302-188,035,547 , GRCh37.p13 chr2: 188,811,029-188,900,274 LINC01090
    nsv5557690sequence alteration1nstd206human GRCh38 chr8: 130,393,596-130,482,687 , GRCh37.p13 chr8: 131,405,842-131,494,933 ASAP1
    nsv5562014sequence alteration1nstd206human GRCh38 chr5: 101,672,221-101,760,888 , GRCh37.p13 chr5: 101,007,925-101,096,592 LOC105379102
    nsv5555079sequence alteration1nstd206human GRCh38 chr6: 104,417,803-104,503,929 , GRCh37.p13 chr6: 104,865,678-104,951,804 LOC105377918
    nsv5554148sequence alteration1nstd206human GRCh38 chrX: 30,476,920-30,560,649 , GRCh37.p13 chrX: 30,495,037-30,578,766 TASL
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