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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5879000copy number variation1nstd209human GRCh38 chr16: 75,546,466-75,571,986 , GRCh37.p13 chr16: 75,580,364-75,605,884 TMEM231, GABARAPL2
    nsv5358359translocation1nstd200human GRCh38 chr16: 75,577,670-75,577,670 , GRCh38 chr16: 75,577,727-75,577,727 , GRCh37.p13 chr16: 75,611,568-75,611,568 , GRCh37.p13 chr16: 75,611,625-75,611,625 GABARAPL2
    nsv5332963translocation1nstd200human GRCh37 chr16: 75,612,114-75,612,114 , GRCh37 chr2: 238,960,237-238,960,237 , GRCh38.p12 chr2: 238,051,596-238,051,596 , GRCh38.p12 chr16: 75,578,216-75,578,216 UBE2F-SCLY, GABARAPL2
    nsv5312413copy number variation1nstd204human GRCh38.p13 chr16: 75,571,209-75,588,620 , GRCh37.p13 chr16: 75,605,107-75,622,518 GABARAPL2
    nsv5300259copy number variation1nstd204human GRCh38.p13 chr16: 75,571,162-75,588,661 , GRCh37.p13 chr16: 75,605,060-75,622,559 GABARAPL2
    nsv5282341copy number variation1nstd204human GRCh38.p13 chr16: 75,570,662-75,572,261 , GRCh37.p13 chr16: 75,604,560-75,606,159 GABARAPL2
    nsv5149349mobile element insertion1nstd203human GRCh38 chr16: 75,574,796-75,574,807 , GRCh37.p13 chr16: 75,608,694-75,608,705 GABARAPL2
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005871copy number variation1nstd200human GRCh38 chr16: 75,551,267-75,905,440 , GRCh37.p13 chr16: 75,585,165-75,939,338 LOC105371347, KARS1, 11 more genes
    nsv5004161copy number variation1nstd200human GRCh38 chr16: 75,574,995-75,575,201 , GRCh37.p13 chr16: 75,608,893-75,609,099 GABARAPL2
    nsv5004160copy number variation1nstd200human GRCh38 chr16: 75,570,115-75,570,197 , GRCh37.p13 chr16: 75,604,013-75,604,095 GABARAPL2
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729987copy number variation1nstd102humanUncertain significance GRCh37 chr16: 75,554,118-75,823,234 , GRCh38.p12 chr16: 75,520,220-75,789,336 LOC105371348, CPHXL2, 10 more genes
    nsv4729944copy number variation1nstd102humanUncertain significance GRCh37 chr16: 75,281,963-75,665,698 , GRCh38.p12 chr16: 75,248,065-75,631,800 KARS1, TMEM170A, 10 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4679571copy number variation1nstd189human GRCh37.p13 chr16: 75,268,553-75,646,894 , GRCh38.p12 chr16: 75,234,655-75,612,996 , CHST6, 10 more genes
    nsv4622615copy number variation1nstd183human GRCh37 chr16: 75,588,506-75,855,475 , GRCh38.p12 chr16: 75,554,608-75,821,577 TERF2IP, ATP5PBP7, 9 more genes
    nsv4457330copy number variation1nstd102humanUncertain significance GRCh37 chr16: 72,677,179-77,439,111 , GRCh38.p12 chr16: 72,643,280-77,405,214 MON1B, PSMD7, 70 more genes
    nsv4456930copy number variation1nstd102humanUncertain significance GRCh37 chr16: 75,275,780-75,684,031 , GRCh38.p12 chr16: 75,241,882-75,650,133 RNU6-758P, ADAT1, 11 more genes
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