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Items: 1 to 20 of 339

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098869copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,586,015-154,774,957 , GRCh38.p12 chrX: 140,503,850-155,545,296 MAGEA6, LOC101928832, 303 more genes
    nsv7098599copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,001,546-154,563,736 , GRCh38.p12 chrX: 153,736,092-155,334,427 TAFAZZIN, LOC105373386, 82 more genes
    nsv7097996copy number variation6nstd102humanPathogenic GRCh37 chrX: 152,014,869-155,171,615 , GRCh38.p12 chrX: 152,846,325-155,941,951 PHF10P1, ZNF185, 132 more genes
    nsv7097995copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 152,014,869-154,563,736 , GRCh38.p12 chrX: 152,846,325-155,334,427 RN7SL697P, CYCSP45, 118 more genes
    nsv7093175copy number variation1nstd102humanPathogenic GRCh38 chrX: 154,805,077-155,030,999 , GRCh37.p13 chrX|NW_003871103.3: 2,239,056-2,464,978 , GRCh37.p13 chrX: 154,033,352-154,259,274 ZNF622P1, H2AB1, 8 more genes
    nsv7079975copy number variation1nstd229human GRCh38 chrX: 154,833,524-154,838,102 , GRCh37.p13 chrX: 154,061,799-154,066,377 , GRCh37.p13 chrX|NW_003871103.3: 2,267,503-2,272,081 SMIM9, F8
    nsv7079974copy number variation1nstd229human GRCh38 chrX: 154,831,801-154,837,200 , GRCh37.p13 chrX|NW_003871103.3: 2,265,780-2,271,179 , GRCh37.p13 chrX: 154,060,076-154,065,475 F8, SMIM9
    nsv7079973copy number variation1nstd229human GRCh38 chrX: 154,831,508-154,831,782 , GRCh37.p13 chrX: 154,059,783-154,060,057 , GRCh37.p13 chrX|NW_003871103.3: 2,265,487-2,265,761 SMIM9
    nsv7079972copy number variation1nstd229human GRCh37.p13 chrX|NW_003871103.3: 2,264,252-2,348,452 , GRCh38 chrX: 154,830,273-154,914,473 , GRCh37.p13 chrX: 154,058,548-154,142,748 F8, EEF1A1P31, 4 more genes
    nsv7079971copy number variation1nstd229human GRCh38 chrX: 154,829,499-154,838,471 , GRCh37.p13 chrX: 154,057,774-154,066,746 , GRCh37.p13 chrX|NW_003871103.3: 2,263,478-2,272,450 SMIM9, F8
    nsv7079970copy number variation1nstd229human GRCh38 chrX: 154,828,856-154,842,109 , GRCh37.p13 chrX|NW_003871103.3: 2,262,835-2,276,088 , GRCh37.p13 chrX: 154,057,131-154,070,384 F8, SMIM9
    nsv7079969copy number variation1nstd229human GRCh38 chrX: 154,828,745-154,838,003 , GRCh37.p13 chrX: 154,057,020-154,066,278 , GRCh37.p13 chrX|NW_003871103.3: 2,262,724-2,271,982 SMIM9, F8
    nsv7079968copy number variation1nstd229human GRCh38 chrX: 154,825,284-154,833,518 , GRCh37.p13 chrX|NW_003871103.3: 2,259,263-2,267,497 , GRCh37.p13 chrX: 154,053,559-154,061,793 SMIM9
    nsv7079967copy number variation1nstd229human GRCh38 chrX: 154,820,204-154,847,589 , GRCh37.p13 chrX|NW_003871103.3: 2,254,183-2,281,568 , GRCh37.p13 chrX: 154,048,479-154,075,864 F8, SMIM9
    nsv7079966copy number variation1nstd229human GRCh38 chrX: 154,818,001-154,867,800 , GRCh37.p13 chrX|NW_003871103.3: 2,251,980-2,301,779 , GRCh37.p13 chrX: 154,046,276-154,096,075 SMIM9, HMGN1P37, 1 more genes
    nsv7079964copy number variation1nstd229human GRCh38 chrX: 154,810,407-155,540,832 , GRCh37.p13 chrX: 154,038,682-154,770,493 , GRCh37.p13 chrX|NW_003871103.3: 2,244,386-2,974,811 LOC101927830, TWF1P2, 25 more genes
    nsv7079963copy number variation1nstd229human GRCh38 chrX: 154,810,201-154,848,100 , GRCh37.p13 chrX|NW_003871103.3: 2,244,180-2,282,079 , GRCh37.p13 chrX: 154,038,476-154,076,375 HMGN1P37, F8, 1 more genes
    nsv7079961copy number variation1nstd229human GRCh38 chrX: 154,800,716-154,976,977 , GRCh37.p13 chrX|NW_003871103.3: 2,234,695-2,410,956 , GRCh37.p13 chrX: 154,028,991-154,205,252 MIR1184-1, SMIM9, 7 more genes
    nsv7079957copy number variation1nstd229human GRCh38 chrX: 154,782,863-155,061,957 , GRCh37.p13 chrX|NW_003871103.3: 2,216,842-2,495,936 , GRCh37.p13 chrX: 154,011,138-154,290,232 SMIM9, CMC4, 9 more genes
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