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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5897531copy number variation1nstd209human GRCh38 chr4: 164,941,888-164,962,694 , GRCh37.p13 chr4: 165,863,040-165,883,846 TRIM61, FAM218A, 2 more genes
    nsv5838407copy number variation1nstd209human GRCh38 chr4: 164,941,822-164,957,762 , GRCh37.p13 chr4: 165,862,974-165,878,914 NACA3P, LOC391711, 2 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5561150sequence alteration1nstd206human GRCh38 chr4: 164,939,786-164,948,273 , GRCh37.p13 chr4: 165,860,938-165,869,425 NACA3P, LOC391710, 1 more genes
    nsv5557699inversion1nstd206human GRCh38 chr4: 164,939,216-164,949,007 , GRCh37.p13 chr4: 165,860,368-165,870,159 NACA3P, LOC391710, 1 more genes
    nsv5387742copy number variation2nstd186human GRCh37 chr4: 165,863,040-165,883,859 , GRCh38.p12 chr4: 164,941,888-164,962,707 FAM218A, NACA3P, 2 more genes
    nsv5381776copy number variation1nstd102humanPathogenic GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127 LOC107986326, LOC107986240, 144 more genes
    nsv5237982copy number variation1nstd204human GRCh38.p13 chr4: 164,941,901-164,962,700 , GRCh37.p13 chr4: 165,863,053-165,883,852 TRIM61, LOC391711, 2 more genes
    nsv5234171copy number variation1nstd204human GRCh38.p13 chr4: 164,941,270-164,954,762 , GRCh37.p13 chr4: 165,862,422-165,875,914 LOC391711, TRIM61, 1 more genes
    nsv5039478inversion1nstd200human GRCh38 chr4: 158,116,539-168,149,530 , GRCh37.p13 chr4: 159,037,691-169,070,681 MIR4454, LOC105377520, 93 more genes
    nsv4948686copy number variation1nstd200human GRCh38 chr4: 164,941,888-164,962,707 , GRCh37.p13 chr4: 165,863,040-165,883,859 TRIM61, FAM218A, 2 more genes
    nsv4948685copy number variation1nstd200human GRCh38 chr4: 164,922,232-164,952,828 , GRCh37.p13 chr4: 165,843,384-165,873,980 NACA3P, LOC391710, 3 more genes
    nsv4948683copy number variation1nstd200human GRCh38 chr4: 164,901,945-165,135,630 , GRCh37.p13 chr4: 165,823,097-166,056,782 LOC100420386, FAM218A, 13 more genes
    nsv4948682copy number variation1nstd200human GRCh38 chr4: 164,888,666-165,010,374 , GRCh37.p13 chr4: 165,809,818-165,931,526 RPL26P16, FAM218BP, 9 more genes
    nsv4948672copy number variation1nstd200human GRCh38 chr4: 164,039,828-165,202,299 , GRCh37.p13 chr4: 164,960,980-166,123,451 MARCHF1, TRIM61, 21 more genes
    nsv4794656copy number variation1nstd200human GRCh37 chr4: 165,863,040-165,883,859 , GRCh38.p12 chr4: 164,941,888-164,962,707 LOC391711, TRIM61, 2 more genes
    nsv4794645copy number variation1nstd200human GRCh37 chr4: 164,960,980-166,123,451 , GRCh38.p12 chr4: 164,039,828-165,202,299 SMIM31, MARCHF1, 21 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
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