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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3922959copy number variation1nstd102humanLikely benign NCBI36 chr17: 3,393,853-3,446,123 , GRCh37 chr17: 3,447,103-3,499,374 , GRCh38 chr17: 3,543,809-3,596,080 TRPV1, TRPV3
    nsv4675240copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,431,968-3,518,264 , GRCh38.p12 chr17: 3,528,674-3,614,970 TRPV1, TRPV3, 1 more genes
    nsv4457478copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,509,831-3,545,112 , GRCh38.p12 chr17: 3,606,537-3,641,818 TRPV1, SHPK, 3 more genes
    nsv5673116copy number variation2nstd102humanPathogenic GRCh37 chr17: 3,392,519-3,564,038 , GRCh38.p12 chr17: 3,489,225-3,660,744 TRPV1, ASPA, 7 more genes
    nsv3889197copy number variation3nstd102humanPathogenic GRCh37 chr17: 3,504,228-3,561,459 , GRCh38 chr17: 3,600,934-3,658,165 TRPV1, CTNS, 4 more genes
    nsv4457673copy number variation2nstd102humanPathogenic GRCh37 chr17: 3,505,567-3,562,748 , GRCh38.p12 chr17: 3,602,273-3,659,454 TRPV1, CTNS, 4 more genes
    nsv6310218copy number variation1nstd102humanPathogenic GRCh37 chr17: 3,504,346-3,561,464 , GRCh38.p12 chr17: 3,601,052-3,658,170 TRPV1, CTNS, 4 more genes
    nsv4457855copy number variation2nstd102humanPathogenic GRCh37 chr17: 3,505,567-3,562,685 , GRCh38.p12 chr17: 3,602,273-3,659,391 TRPV1, CTNS, 4 more genes
    nsv3909792copy number variation3nstd102humanPathogenic GRCh37 chr17: 3,505,567-3,557,452 , GRCh38.p12 chr17: 3,602,273-3,654,158 TRPV1, CTNS, 4 more genes
    nsv4457790copy number variation4nstd102humanUncertain significance, Pathogenic GRCh37 chr17: 3,505,567-3,557,441 , GRCh38.p12 chr17: 3,602,273-3,654,147 TRPV1, CTNS, 4 more genes
    nsv4457725copy number variation6nstd102humanPathogenic GRCh37 chr17: 3,505,567-3,557,440 , GRCh38.p12 chr17: 3,602,273-3,654,146 TRPV1, CTNS, 4 more genes
    nsv4457746copy number variation2nstd102humanPathogenic GRCh37 chr17: 3,505,975-3,557,440 , GRCh38.p12 chr17: 3,602,681-3,654,146 TRPV1, CTNS, 4 more genes
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 TRPV1, RPS4XP17, 289 more genes
    nsv3915884copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-6,862,369 , GRCh38 chr17: 162,088-6,959,050 , NCBI36 chr17: 11,879-6,803,093 TRPV1, LOC105371592, 222 more genes
    nsv3922546copy number variation1nstd102humanPathogenic NCBI36 chr17: 525-5,779,421 , GRCh38 chr17: 150,732-5,935,377 , GRCh37 chr17: 525-5,838,697 TRPV1, CHRNE, 198 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 TRPV1, SRR, 196 more genes
    nsv3913795copy number variation1nstd102humanPathogenic NCBI36 chr17: 43,098-5,496,266 , GRCh37 chr17: 45,835-5,555,542 , GRCh38 chr17: 193,307-5,652,222 TRPV1, BHLHA9, 194 more genes
    nsv3921779copy number variation1nstd102humanPathogenic NCBI36 chr17: 87,039-4,585,577 , GRCh38 chr17: 237,248-4,735,533 , GRCh37 chr17: 396,627-4,638,828 TRPV1, ARRB2, 146 more genes
    nsv3919819copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-4,168,935 , NCBI36 chr17: 48,539-4,115,684 , GRCh38 chr17: 198,748-4,265,640 TRPV1, LOC105371430, 125 more genes
    nsv3904699copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-3,871,323 , GRCh38.p12 chr17: 157,423-3,968,029 TRPV1, OVCA2, 120 more genes
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