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Items: 1 to 20 of 157

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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
    nsv7144894insertion1nstd232human GRCh37.p13 chr17: 26,942,268-26,942,268 , GRCh38.p12 chr17: 28,615,250-28,615,250 BLTP2, SPAG5-AS1
    nsv7140767insertion1nstd232human GRCh37.p13 chr17: 26,931,098-26,931,098 , GRCh38.p12 chr17: 28,604,080-28,604,080 SPAG5-AS1
    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
    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
    nsv6985414copy number variation1nstd229human GRCh38 chr17: 28,599,271-28,601,026 , GRCh37.p13 chr17: 26,926,289-26,928,044 SPAG5, SPAG5-AS1
    nsv6983677copy number variation1nstd229human GRCh38 chr17: 28,389,847-28,690,853 , GRCh37.p13 chr17: 26,840,020-27,017,871 LOC101060112, SPAG5, 15 more genes
    nsv6979168copy number variation1nstd229human GRCh38 chr17: 28,603,666-28,603,967 , GRCh37.p13 chr17: 26,930,684-26,930,985 SPAG5-AS1
    nsv6582795inversion1nstd223human GRCh38 chr17: 28,600,581-28,601,149 , GRCh37.p13 chr17: 26,927,599-26,928,167 SPAG5-AS1
    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
    nsv6504368copy number variation1nstd223human GRCh38 chr17: 28,595,177-28,597,304 , GRCh37.p13 chr17: 26,922,195-26,924,322 SPAG5-AS1, SPAG5
    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
    nsv6288509insertion1nstd214human GRCh38 chr17: 28,604,080-28,604,080 , GRCh37.p13 chr17: 26,931,098-26,931,098 SPAG5-AS1
    nsv6250719mobile element insertion1nstd215human GRCh38 chr17: 28,603,492-28,603,492 , GRCh37.p13 chr17: 26,930,510-26,930,510 SPAG5-AS1
    nsv6193577copy number variation1nstd214human GRCh38 chr17: 28,604,021-28,604,245 , GRCh37.p13 chr17: 26,931,039-26,931,263 SPAG5-AS1
    nsv6191793copy number variation1nstd214human GRCh38 chr17: 28,604,056-28,604,280 , GRCh37.p13 chr17: 26,931,074-26,931,298 SPAG5-AS1
    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
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