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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097585copy number variation1nstd102humanUncertain significance GRCh37 chr6: 72,984,032-73,001,769 , GRCh38.p12 chr6: 72,274,329-72,292,066 RIMS1
    nsv7097082copy number variation1nstd102humanUncertain significance GRCh37 chr6: 72,889,258-73,332,335 , GRCh38.p12 chr6: 72,179,555-72,622,607 LOC643067, KCNQ5, 5 more genes
    nsv7097081copy number variation1nstd102humanUncertain significance GRCh37 chr6: 72,678,666-72,678,786 , GRCh38.p12 chr6: 71,968,963-71,969,083 RIMS1
    nsv7097080copy number variation1nstd102humanUncertain significance GRCh37 chr6: 72,596,727-72,984,155 , GRCh38.p12 chr6: 71,887,024-72,274,452 RIMS1
    nsv7054109inversion1nstd229human GRCh38 chr6: 71,923,107-71,928,304 , GRCh37.p13 chr6: 72,632,810-72,638,007 RIMS1
    nsv7049523inversion1nstd229human GRCh38 chr6: 71,947,820-71,947,859 , GRCh37.p13 chr6: 72,657,523-72,657,562 RIMS1
    nsv7049199inversion1nstd229human GRCh38 chr6: 72,118,025-72,118,118 , GRCh37.p13 chr6: 72,827,728-72,827,821 RIMS1
    nsv7046020inversion1nstd229human GRCh38 chr6: 71,927,805-71,930,130 , GRCh37.p13 chr6: 72,637,508-72,639,833 RIMS1
    nsv7044588inversion1nstd229human GRCh38 chr6: 72,020,858-72,020,936 , GRCh37.p13 chr6: 72,730,561-72,730,639 RIMS1
    nsv7042725inversion1nstd229human GRCh38 chr6: 71,995,236-72,003,482 , GRCh37.p13 chr6: 72,704,939-72,713,185 RIMS1
    nsv6797356copy number variation1nstd229human GRCh38 chr6: 71,999,277-72,014,291 , GRCh37.p13 chr6: 72,708,980-72,723,994 RIMS1
    nsv6797006copy number variation1nstd229human GRCh38 chr6: 72,154,151-72,163,835 , GRCh37.p13 chr6: 72,863,854-72,873,538 RIMS1
    nsv6796882copy number variation1nstd229human GRCh38 chr6: 72,149,936-72,156,161 , GRCh37.p13 chr6: 72,859,639-72,865,864 RIMS1
    nsv6796857copy number variation1nstd229human GRCh38 chr6: 72,015,001-72,019,300 , GRCh37.p13 chr6: 72,724,704-72,729,003 RIMS1
    nsv6796343copy number variation1nstd229human GRCh38 chr6: 72,148,373-72,150,431 , GRCh37.p13 chr6: 72,858,076-72,860,134 RIMS1
    nsv6795855copy number variation1nstd229human GRCh38 chr6: 71,928,112-71,944,416 , GRCh37.p13 chr6: 72,637,815-72,654,119 RIMS1
    nsv6795377copy number variation1nstd229human GRCh38 chr6: 71,960,801-71,965,800 , GRCh37.p13 chr6: 72,670,504-72,675,503 RIMS1
    nsv6794434copy number variation1nstd229human GRCh38 chr6: 72,339,277-72,350,896 , GRCh37.p13 chr6: 73,048,980-73,060,598 RIMS1
    nsv6793545copy number variation1nstd229human GRCh38 chr6: 71,980,701-71,989,100 , GRCh37.p13 chr6: 72,690,404-72,698,803 RIMS1
    nsv6793071copy number variation1nstd229human GRCh38 chr6: 71,946,501-71,960,900 , GRCh37.p13 chr6: 72,656,204-72,670,603 RIMS1
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