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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148088copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,263,507-27,829,791 , GRCh38.p12 chr17: 26,936,481-29,502,773 RNU4-34P, RNU6-711P, 95 more genes
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7094962copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-27,581,367 , GRCh38.p12 chr17: 28,357,671-29,254,349 FLOT2, SPAG5-AS1, 50 more genes
    nsv7076914inversion1nstd229human GRCh38 chr17: 28,733,178-28,737,947 , GRCh37.p13 chr17: 27,060,196-27,064,965 NEK8
    nsv7067872inversion1nstd229human GRCh38 chr17: 28,416,471-28,817,211 , GRCh37.p13 chr17: 26,840,020-27,144,229 SUPT6H, SPAG5-AS1, 25 more genes
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv6990526copy number variation1nstd229human GRCh38 chr17: 28,743,522-28,743,571 , GRCh37.p13 chr17: 27,070,540-27,070,589 NEK8, TRAF4
    nsv6978596copy number variation1nstd229human GRCh38 chr17: 28,732,597-28,749,556 , GRCh37.p13 chr17: 27,059,615-27,076,574 TRAF4, NEK8
    nsv6515002copy number variation1nstd223human GRCh38 chr17: 28,371,101-28,759,756 , GRCh37.p13 chr17: 26,840,020-27,086,774 FAM222B, SDF2, 26 more genes
    nsv6314042copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-28,281,232 , GRCh38.p12 chr17: 22,164,047-29,954,214 TAOK1, TNFAIP1, 131 more genes
    nsv6133349copy number variation1nstd213human GRCh37 chr17: 26,970,000-27,060,001 , GRCh38.p12 chr17: 28,642,982-28,732,983 RPL23A, SDF2, 11 more genes
    nsv6133232copy number variation1nstd213human GRCh37 chr17: 26,970,000-27,750,001 , GRCh38.p12 chr17: 28,642,982-29,422,983 CRYBA1, FLOT2, 37 more genes
    nsv6133229copy number variation1nstd213human GRCh37 chr17: 25,300,000-32,120,001 , GRCh38.p12 chr17: 26,972,974-33,792,982 BLMH, CPD, 197 more genes
    nsv6133228copy number variation1nstd213human GRCh37 chr17: 25,300,000-27,290,001 , GRCh38.p12 chr17: 26,972,974-28,962,983 LGALS9, RPL23A, 82 more genes
    nsv5353966translocation1nstd200human GRCh38 chr17: 28,735,181-28,735,181 , GRCh38 chr8: 3,226,809-3,226,809 , GRCh37.p13 chr8: 3,084,331-3,084,331 , GRCh37.p13 chr17: 27,062,199-27,062,199 CSMD1, NEK8
    nsv5353965translocation1nstd200human GRCh38 chr8: 3,226,544-3,226,544 , GRCh38 chr17: 28,735,173-28,735,173 , GRCh37.p13 chr17: 27,062,191-27,062,191 , GRCh37.p13 chr8: 3,084,066-3,084,066 CSMD1, NEK8
    nsv5330314translocation1nstd200human GRCh37 chr17: 27,062,199-27,062,199 , GRCh37 chr8: 3,084,331-3,084,331 , GRCh38.p12 chr17: 28,735,181-28,735,181 , GRCh38.p12 chr8: 3,226,809-3,226,809 CSMD1, NEK8
    nsv5329799translocation1nstd200human GRCh37 chr17: 27,062,191-27,062,191 , GRCh37 chr8: 3,084,066-3,084,066 , GRCh38.p12 chr8: 3,226,544-3,226,544 , GRCh38.p12 chr17: 28,735,173-28,735,173 CSMD1, NEK8
    nsv5189346mobile element insertion1nstd203human GRCh38 chr17: 28,729,357-28,729,373 , GRCh37.p13 chr17: 27,056,375-27,056,391 NEK8
    nsv5154093mobile element insertion1nstd203human GRCh38 chr17: 28,736,528-28,736,542 , GRCh37.p13 chr17: 27,063,546-27,063,560 NEK8
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