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Items: 1 to 20 of 519

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960718insertion1nstd209human GRCh38 chr4: 98,533,939-98,533,939 , GRCh37.p13 chr4: 99,455,090-99,455,090 TSPAN5
    nsv5957809insertion1nstd209human GRCh38 chr4: 98,555,986-98,555,986 , GRCh37.p13 chr4: 99,477,137-99,477,137 TSPAN5
    nsv5906265copy number variation1nstd209human GRCh38 chr4: 98,494,406-98,494,495 , GRCh37.p13 chr4: 99,415,557-99,415,646 TSPAN5
    nsv5900374copy number variation1nstd209human GRCh38 chr4: 98,489,701-98,489,758 , GRCh37.p13 chr4: 99,410,852-99,410,909 TSPAN5
    nsv5893919copy number variation1nstd209human GRCh38 chr4: 98,489,805-98,491,855 , GRCh37.p13 chr4: 99,410,956-99,413,006 TSPAN5
    nsv5892472copy number variation1nstd209human GRCh38 chr4: 98,626,126-98,626,177 , GRCh37.p13 chr4: 99,547,277-99,547,328 TSPAN5
    nsv5840234copy number variation1nstd209human GRCh38 chr4: 98,489,825-98,491,860 , GRCh37.p13 chr4: 99,410,976-99,413,011 TSPAN5
    nsv5690800mobile element insertion1nstd211human GRCh38 chr4: 98,531,743-98,531,743 , GRCh37.p13 chr4: 99,452,894-99,452,894 TSPAN5
    nsv5677197mobile element insertion2nstd211human GRCh38 chr4: 98,533,962-98,533,962 , GRCh37.p13 chr4: 99,455,113-99,455,113 TSPAN5
    nsv5674551mobile element insertion1nstd211human GRCh38 chr4: 98,552,973-98,552,973 , GRCh37.p13 chr4: 99,474,124-99,474,124 TSPAN5
    nsv5619195insertion1nstd207human GRCh38 chr4: 98,617,148-98,617,148 , GRCh37.p13 chr4: 99,538,299-99,538,299 TSPAN5
    nsv5569560copy number variation1nstd207human GRCh38 chr4: 98,626,126-98,626,177 , GRCh37.p13 chr4: 99,547,277-99,547,328 TSPAN5
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5472902copy number variation1nstd206human GRCh38 chr4: 98,541,402-98,547,788 , GRCh37.p13 chr4: 99,462,553-99,468,939 TSPAN5
    nsv5470593copy number variation1nstd206human GRCh38 chr4: 98,498,320-98,501,849 , GRCh37.p13 chr4: 99,419,471-99,423,000 TSPAN5
    nsv5464332copy number variation1nstd206human GRCh38 chr4: 98,556,812-98,562,437 , GRCh37.p13 chr4: 99,477,963-99,483,588 TSPAN5
    nsv5461789copy number variation1nstd206human GRCh38 chr4: 98,489,805-98,491,856 , GRCh37.p13 chr4: 99,410,956-99,413,007 TSPAN5
    nsv5457205copy number variation1nstd206human GRCh38 chr4: 98,585,381-98,592,100 , GRCh37.p13 chr4: 99,506,532-99,513,251 TSPAN5
    nsv5411489mobile element insertion1nstd206human GRCh38 chr4: 98,531,743-98,531,785 , GRCh37.p13 chr4: 99,452,894-99,452,936 TSPAN5
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