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Items: 1 to 20 of 224

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5896495copy number variation1nstd209human GRCh38 chr4: 155,327,538-155,341,634 , GRCh37.p13 chr4: 156,248,690-156,262,786 MAP9
    nsv5607492insertion1nstd207human GRCh38 chr4: 155,349,247-155,349,247 , GRCh37.p13 chr4: 156,270,399-156,270,399 MAP9
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5541682insertion1nstd206human GRCh38 chr4: 155,349,248-155,349,248 , GRCh37.p13 chr4: 156,270,400-156,270,400 MAP9
    nsv5353322translocation1nstd200human GRCh38 chr4: 155,365,950-155,365,950 , GRCh38 chr4: 155,365,258-155,365,258 , GRCh37.p13 chr4: 156,286,410-156,286,410 , GRCh37.p13 chr4: 156,287,102-156,287,102 MAP9
    nsv5315217copy number variation1nstd204human GRCh38.p13 chr4: 155,363,239-155,366,392 , GRCh37.p13 chr4: 156,284,391-156,287,544 MAP9
    nsv5240097copy number variation1nstd204human GRCh38.p13 chr4: 155,363,223-155,366,254 , GRCh37.p13 chr4: 156,284,375-156,287,406 MAP9
    nsv5226795copy number variation1nstd204human GRCh38.p13 chr4: 155,349,701-155,353,400 , GRCh37.p13 chr4: 156,270,853-156,274,552 MAP9-AS1, MAP9
    nsv5222028copy number variation1nstd204human GRCh38.p13 chr4: 155,341,801-155,345,600 , GRCh37.p13 chr4: 156,262,953-156,266,752 MAP9
    nsv5086235mobile element insertion1nstd203human GRCh38 chr4: 155,366,559-155,366,570 , GRCh37.p13 chr4: 156,287,711-156,287,722 MAP9
    nsv4929795copy number variation1nstd200human GRCh38 chr4: 155,372,729-155,382,888 , GRCh37.p13 chr4: 156,293,881-156,304,040 YWHAEP4, MAP9, 1 more genes
    nsv4929794copy number variation1nstd200human GRCh38 chr4: 155,337,924-155,347,265 , GRCh37.p13 chr4: 156,259,076-156,268,417 MAP9
    nsv4801246copy number variation1nstd200human GRCh37 chr4: 156,293,881-156,304,040 , GRCh38.p12 chr4: 155,372,729-155,382,888 YWHAEP4, MAP9, 1 more genes
    nsv4801245copy number variation1nstd200human GRCh37 chr4: 156,286,410-156,287,102 , GRCh38.p12 chr4: 155,365,258-155,365,950 MAP9
    nsv4801244copy number variation1nstd200human GRCh37 chr4: 156,259,076-156,268,417 , GRCh38.p12 chr4: 155,337,924-155,347,265 MAP9
    nsv4768764insertion1nstd186human GRCh37 chr4: 156,270,401-156,270,401 , GRCh38.p12 chr4: 155,349,249-155,349,249 MAP9
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
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