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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4360197copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr22: 32,494,428-49,525,271 , GRCh37.p13 chr22: 34,164,428-51,178,405 , GRCh38.p12 chr22: 33,768,441-50,739,977 RAC2, ACR, 470 more genes
    nsv4360194copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr22: 15,777,498-49,525,130 , GRCh37.p13 chr22: 17,397,498-51,178,264 , GRCh38.p12 chr22: 16,916,608-50,739,836 RAC2, ACO2, 1104 more genes
    nsv4359385copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr22: 34,794,118-36,728,335 , GRCh37.p13 chr22: 36,464,172-38,398,389 , GRCh38.p12 chr22: 36,068,124-38,002,382 RAC2, CSF2RB, 76 more genes
    nsv4356096copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr22: 35,630,818-36,281,463 , GRCh37.p13 chr22: 37,300,872-37,951,517 , GRCh38.p12 chr22: 36,904,830-37,555,510 RAC2, SSTR3, 21 more genes
    nsv4354594copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr22: 35,850,235-36,306,710 , GRCh37.p13 chr22: 37,520,289-37,976,764 , GRCh38.p12 chr22: 37,124,249-37,580,757 RAC2, MFNG, 12 more genes
    nsv4352665copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr22: 15,777,633-49,525,079 , GRCh37.p13 chr22: 17,397,633-51,178,213 , GRCh38.p12 chr22: 16,916,743-50,739,785 RAC2, ADORA2A, 1104 more genes
    nsv4351920copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr22: 35,278,369-36,395,868 , GRCh37.p13 chr22: 36,948,423-38,065,922 , GRCh38.p12 chr22: 36,552,376-37,669,915 RAC2, CSF2RB, 35 more genes
    nsv4351691copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr22: 34,059,986-37,626,128 , GRCh37.p13 chr22: 35,729,986-39,296,182 , GRCh38.p12 chr22: 35,333,993-38,900,177 RAC2, HMOX1, 124 more genes
    nsv4351631copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr22: 35,787,755-49,524,226 , GRCh37.p13 chr22: 37,457,809-51,177,360 , GRCh38.p12 chr22: 37,061,769-50,738,932 RAC2, ACO2, 398 more genes
    nsv4278013copy number variation1nstd166human GRCh37.p13 chr22: 37,381,892-38,500,309 , GRCh38.p12 chr22: 36,985,851-38,104,302 RAC2, IL2RB, 46 more genes
    nsv4044497mobile element insertion1nstd166human GRCh37.p13 chr22: 26,765,044-42,917,773 , GRCh38.p12 chr22: 26,369,078-42,521,767 RAC2, ADSL, 463 more genes
    nsv3936634insertion1nstd167human GRCh37 (hg19) chr22: 37,623,242-37,623,242 , GRCh38.p12 chr22: 37,227,202-37,227,202 RAC2
    nsv3925926insertion1nstd167human GRCh37 (hg19) chr22: 37,623,494-37,623,494 , GRCh38.p12 chr22: 37,227,454-37,227,454 RAC2
    nsv3919085copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr22: 17,008,132-49,591,432 , GRCh37.p13 chr22: 18,628,132-51,203,353 , GRCh38.p12 chr22: 18,145,365-50,806,138 RAC2, PNPLA5, 1068 more genes
    nsv3907231copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964 , NCBI36 (hg18) chr22: 14,494,244-49,558,258 RAC2, GRK3, 1147 more genes
    nsv3906962copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr22: 35,728,929-51,220,961 , GRCh38.p12 chr22: 35,332,936-50,782,533 , NCBI36 (hg18) chr22: 34,058,929-49,567,827 RAC2, CYB5R3, 456 more genes
    nsv3904443copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr22: 36,877,226-38,548,989 , GRCh38.p12 chr22: 36,481,179-38,152,982 , NCBI36 (hg18) chr22: 35,207,172-36,878,935 RAC2, H1F0, 64 more genes
    nsv3902776copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007 , NCBI36 (hg18) chr22: 14,434,667-49,590,301 RAC2, ADORA2A, 1149 more genes
    nsv3902598copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474 , NCBI36 (hg18) chr22: 14,434,691-49,567,768 RAC2, GRK3, 1149 more genes
    nsv3899772copy number variation1nstd102humanUncertain significance GRCh37 (hg19) chr22: 37,090,025-39,601,950 , GRCh38.p12 chr22: 36,693,980-39,205,945 , NCBI36 (hg18) chr22: 35,419,971-37,931,896 RAC2, CSNK1E, 100 more genes
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