adprm[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3897666	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 10,583,805-10,633,471 , GRCh38.p12 chr17: 10,680,488-10,730,154	ADPRM, TMEM220, 3 more genes
nsv7095073	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 10,436,582-10,600,824 , GRCh38.p12 chr17: 10,533,265-10,697,507	ADPRM, MYH3, 3 more genes
nsv7095074	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 10,531,970-10,600,824 , GRCh38.p12 chr17: 10,628,653-10,697,507	ADPRM, SCO1, 1 more genes
nsv3917187	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 10,178,551-10,744,358 , GRCh37 chr17: 10,237,826-10,803,633 , GRCh38 chr17: 10,334,509-10,900,316	ADPRM, MYH2, 14 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	ADPRM, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	ADPRM, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	ADPRM, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	ADPRM, SMURF2, 2366 more genes
nsv3897625	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420	ADPRM, GP1BA, 439 more genes
nsv3915354	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519	ADPRM, KIF1C-AS1, 433 more genes
nsv3917059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901	ADPRM, PSMB6, 409 more genes
nsv7148254	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413	ADPRM, RFLNB, 401 more genes
nsv3904771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115	ADPRM, SLC2A4, 401 more genes
nsv3911050	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391	ADPRM, C17orf49, 209 more genes
nsv3895307	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 10,583,589-10,698,588 , GRCh38.p12 chr17: 10,680,272-10,795,271	ADPRM, TMEM220-AS1, 4 more genes
nsv4457480	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 10,604,119-10,744,366 , GRCh38.p12 chr17: 10,700,802-10,841,049	ADPRM, TMEM220, 4 more genes
nsv4684245	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 10,493,837-15,099,023 , GRCh38.p12 chr17: 10,590,520-15,195,706	ADPRM, LOC100506974, 52 more genes
nsv1398516	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 9,701,182-11,983,353 , GRCh37 chr17: 9,604,499-11,886,670	ADPRM, SCO1, 29 more genes
nsv3921439	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 10,520,697-11,183,346 , GRCh37.p13 chr17: 10,579,972-11,242,621 , GRCh38.p12 chr17: 10,676,655-11,339,304	ADPRM, RNU6-1065P, 11 more genes
nsv3922092	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 10,288,853-10,894,231 , GRCh37.p13 chr17: 10,348,128-10,953,506 , GRCh38.p12 chr17: 10,444,811-11,050,189	ADPRM, MYH3, 13 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 22

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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